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EP3965822A1 - Adc for a treatment concomitant with or subsequent to docetaxel - Google Patents

Adc for a treatment concomitant with or subsequent to docetaxel

Info

Publication number
EP3965822A1
EP3965822A1 EP20722599.6A EP20722599A EP3965822A1 EP 3965822 A1 EP3965822 A1 EP 3965822A1 EP 20722599 A EP20722599 A EP 20722599A EP 3965822 A1 EP3965822 A1 EP 3965822A1
Authority
EP
European Patent Office
Prior art keywords
seq
adc
sequence
antibody
docetaxel
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP20722599.6A
Other languages
German (de)
French (fr)
Inventor
Alexandra Jouhanneaud
Liliane Goetsch
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pierre Fabre Medicament SA
Original Assignee
Pierre Fabre Medicament SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pierre Fabre Medicament SA filed Critical Pierre Fabre Medicament SA
Publication of EP3965822A1 publication Critical patent/EP3965822A1/en
Withdrawn legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/337—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
    • A—HUMAN NECESSITIES
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    • A61K31/28—Compounds containing heavy metals
    • A61K31/282—Platinum compounds
    • A—HUMAN NECESSITIES
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    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
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    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
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    • A61K31/704—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin
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    • A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
    • A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
    • A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
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    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
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    • A—HUMAN NECESSITIES
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    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6801—Drug-antibody or immunoglobulin conjugates defined by the pharmacologically or therapeutically active agent
    • A61K47/6803—Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates
    • A—HUMAN NECESSITIES
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    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6801—Drug-antibody or immunoglobulin conjugates defined by the pharmacologically or therapeutically active agent
    • A61K47/6803—Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates
    • A61K47/68031—Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates the drug being an auristatin
    • A—HUMAN NECESSITIES
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    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6801—Drug-antibody or immunoglobulin conjugates defined by the pharmacologically or therapeutically active agent
    • A61K47/6803—Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates
    • A61K47/6811—Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates the drug being a protein or peptide, e.g. transferrin or bleomycin
    • A61K47/6817—Toxins
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    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6835—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
    • A61K47/6849—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a receptor, a cell surface antigen or a cell surface determinant
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2863—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against receptors for growth factors, growth regulators
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    • A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Definitions

  • the present invention relates to the use of an anti-IGF1 R ADC (ADC-A) for the treatment of proliferative diseases, such as cancer, characterized in that ADC-A is administered concomitantly or subsequently to docetaxel.
  • ADC-A anti-IGF1 R ADC
  • hyperproliferative diseases such as cancer
  • the treatment of hyperproliferative diseases constitutes a real public health challenge.
  • the first thing is to find effective anti-tumor drugs. But it is also a matter of providing long-term solutions in the event of the appearance of resistance, a frequent phenomenon, to these first treatments.
  • Docetaxel is a diterpene used as an anti-cancer medicine that acts on the microtubules of cancer cells and results in the blocking of mitosis.
  • the efficacy of docetaxel has been proven in quite a number of tumors including breast cancer, lung cancer, prostate cancer. However, over time a large number of patients develop resistance to docetaxel leading to treatment failure.
  • IGF-1 R The insulin-like growth factor 1 receptor referred to as IGF-1 R (or IGF1 R) is a receptor with tyrosine kinase activity having 70% homology to the insulin receptor IR.
  • IGF-IR is a glycoprotein with a molecular weight of approximately 350,000. It is a heterotetrameric receptor in which each half - linked by disulfide bonds - is composed of an extracellular ⁇ subunit and a subunit. transmembrane unit b.
  • IGF-IR binds IGF1 and IGF2 with very high affinity (Kd # 1 nM) and is able to bind to insulin with 100 to 1000 times lower affinity.
  • Cytoplasmic protein tyrosine kinases are activated by ligand binding to the extracellular domain of IGF-1 R. Activation of these kinases in turn results in the activation of various intracellular substrates, including IRS-1, IRS-2, She and Grb 10.
  • the 1RS proteins are involved, through the activation of numerous downstream effectors, in numerous pathways inducing cell growth and differentiation. It seems, moreover, that the pathway mainly involved in the protection against apoptosis is the path of phosphatidyl-inositol 3-kinases (PI3-kinases).
  • IGF-IR Activation of IGF-IR leads, in a wide variety of cells, to independent abnormal cell growth and tumor formation. IGF-IR is thus expressed in a wide variety of tumors and tumor lines.
  • ADC antibody-drug conjugate
  • the present invention has made it possible to show that the use of an anti-IGF1 R ADC in combination with docetaxel makes it possible to obtain a synergistic effect in the treatment of tumors. Equally surprisingly, it has been shown that the use of an anti-IGF1 R ADC can treat tumors that have become resistant after treatment with docetaxel.
  • FIG 1 Evolution of the average tumor volume in mm 3 as a function of time in days in mice bearing an MCF-7 tumor of approximately 150 mm 3 after A.
  • a subject of the present invention is thus an anti-IGF1 R ADC (ADC-A) for its use in the treatment of proliferative diseases, such as cancer, characterized in that ADC-A is administered concomitantly or subsequently to docetaxel .
  • a subject of the present invention is also the use of an anti-IGF1 R ADC (ADC-A) for the treatment of proliferative diseases, such as cancer, characterized in that ADC-A is administered concomitantly or subsequently to docetaxel.
  • the present invention also relates to the use of an anti-IGF1 R ADC
  • ADC-A for the preparation of a medicament for the treatment of proliferative diseases, such as cancer, characterized in that ADC-A is administered concomitantly or subsequently with docetaxel.
  • the present invention also relates to a method of treating a proliferative disease, such as cancer, comprising administering to a patient in need an effective amount of an anti-IGF1 R ADC (ADC-A). and docetaxel, characterized in that ADC-A is administered concomitantly or subsequent to docetaxel.
  • ADC-A anti-IGF1 R ADC
  • docetaxel according to the invention, is meant the compound of the following formula:
  • Docetaxel is notably sold under the brand name Taxotere®.
  • pharmaceutically acceptable is meant that which is useful in the preparation of a pharmaceutical composition which is generally safe, non-toxic and neither biologically nor otherwise undesirable and which is acceptable for veterinary use as well as human pharmaceutical.
  • pharmaceutically acceptable salt or solvate of a compound is meant a salt or solvate which is pharmaceutically acceptable, as defined herein, and which has the desired pharmacological activity of the parent compound.
  • compositions include in particular:
  • the pharmaceutically acceptable acid addition salts formed with pharmaceutically acceptable inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid and the like; or formed with pharmaceutically acceptable organic acids such as formic acid, acetic acid, benzenesulfonic acid, benzoic acid, camphorsulfonic acid, citric acid, ethanesulfonic acid, fumaric acid, glucoheptonic acid, gluconic acid, glutamic acid, glycolic acid, hydroxynaphthoic acid, 2-hydroxyethanesulfonic acid, lactic acid, maleic acid, malic acid, l 'mandelic acid, methanesulfonic acid, muconic acid, 2-naphthalenesulfonic acid, propionic acid, salicylic acid, succinic acid, dibenzoyl-L-tartaric acid, tartaric acid, p-toluenesulfonic acid, trimethylacetic acid,
  • a metal ion for example an alkali metal ion, an alkaline earth ion or a d ion.
  • aluminum is coordinated with a pharmaceutically acceptable organic base such as diethanolamine, ethanolamine, N-methylglucamine, triethanolamine, tromethamine and the like; or with a pharmaceutically acceptable inorganic base such as aluminum hydroxide, calcium hydroxide, potassium hydroxide, sodium carbonate, sodium hydroxide and the like.
  • Solvates acceptable for the pharmaceutical use of the compounds according to the present invention include conventional solvates such as those formed, during the last step of the process for preparing the compounds according to the invention, with the reaction solvent (s).
  • solvates formed with water commonly called hydrates
  • ethanol it may be, for example, a trihydrate.
  • ADC-A is an anti-IGF1 R ADC of the following formula
  • Ab is an anti-IGF1 R antibody comprising the three CDRs (complementarity determining regions) of heavy chains of sequences SEQ ID No 1, 2 and 3 and the three CDRs of light chain of sequences SEQ ID No 4, 5 and 6, and n is between 1 and 12, in particular is equal to 2 or 4.
  • antibody refers to any suitable immunoglobulin.
  • monoclonal antibodies isolated, modified or recombinant antibodies (for example, monoclonal antibodies complete or intact), polyclonal antibodies, multivalent antibodies or multispecific antibodies (e.g. bispecific antibodies) as well as antibody fragments thereof, provided that they exhibit the desired biological activity, in particular the fragments thereof binding to the antigen. They are more particularly monoclonal antibodies or possibly fragments thereof which bind to the antigen.
  • antigen-binding fragment of an antibody according to the invention is intended to indicate any peptide, polypeptide or protein which retains the ability to bind to the target (also generally called antigen) of the antibody.
  • anti-IGF-1 R antibody denotes an antibody capable of binding to IGF-1 R, more particularly to an epitope located in IGF-1 R, preferably the domain extracellular IGF-1 R, more preferably human IGF-1 R (SEQ ID No 50) and still more preferably the extracellular domain of human IGF-1 R (SEQ ID No 51), and still more preferably the N-terminal part of the extracellular domain of human IGF-1R (SEQ ID No 52), or any of its naturally occurring variant sequences.
  • the antibody according to the invention comprises the three CDRs of heavy chains comprising or consisting of the sequences SEQ ID No 1, 2 and 3, or any sequence having at least 80%, of preferably 85%, 90%, 95% and 98% identity with SEQ ID No 1, 2 or 3; and the three CDRs of light chains comprising or consisting of the sequences SEQ ID No 4, 5 and 6, or any sequence having at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No 4, 5 or 6.
  • the percentages of identity to which reference is made in the context of the disclosure of the present invention are determined on the basis of an overall alignment of the sequences to be compared, that is to say on an alignment of the sequences taken in their entirety over the entire length using any algorithm well known to those skilled in the art such as the algorithm of Needleman and Wunsch-1970.
  • This sequence comparison can be performed using any software well known to those skilled in the art: for example the needle software using the “Gap open” parameter equal to 10.0, the “Gap extend” parameter equal to 0.5 and a “Blosum 62” matrix.
  • the needle software is for example available on the ebi.ac.uk world wide website under the name “Align”.
  • the antibody according to the invention has an amino acid sequence which is not 100% identical to the reference sequence but which has at least 80%, preferably 85%, 90%, 95% and 98% d 'identity with such a reference sequence, it may present insertions, deletions or substitutions with respect to the reference sequence.
  • the substitution is preferably carried out by an “equivalent” amino acid, that is to say any amino acid whose structure is close to that of the original amino acid and is therefore unlikely to modify the biological activities of the antibody. Examples of such substitutions are shown in the following table:
  • the antibody is a murine antibody characterized in that it also comprises constant regions of light chain and of heavy chain derived from an antibody of a heterologous species in mice, in particular humans.
  • the antibody is a chimeric antibody (c) characterized in that it also comprises constant regions of light and heavy chains derived from an antibody of a species heterologous with the mouse, in particular human.
  • a chimeric antibody is an antibody containing a natural variable region (light chain and heavy chain) derived from an antibody of a given species in combination with constant regions of the light chain and the heavy chain of an antibody of a species heterologous to said given species.
  • the antibody is chosen from:
  • the antibody is chosen from:
  • an antibody comprising a heavy chain variable domain of sequence SEQ ID No 13 or any sequence having at least 80% identity with SEQ ID No
  • an antibody comprising a heavy chain variable domain of sequence SEQ ID No 14 or any sequence having at least 80% identity with SEQ ID No
  • an antibody comprising a heavy chain variable domain of sequence SEQ ID No 15 or any sequence having at least 80% identity with SEQ ID No 15 and the three light chain CDRs of sequences SEQ ID No 9, 5 and 12;
  • an antibody comprising a heavy chain variable domain of sequence SEQ ID No 16 or any sequence having at least 80% identity with SEQ ID No
  • any sequence exhibiting at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No 13 to 17 is meant respectively the sequences exhibiting the three CDRs with heavy chains SEQ ID No 1, 2 and 3 and, in addition, exhibiting at least 80%, preferably 85%, 90%, 95% and 98%, identity with the complete sequence SEQ ID No 13 to 17 apart from the sequences corresponding to the CDRs (i.e. SEQ ID No 1, 2 and 3).
  • the antibody is chosen from:
  • the antibody is chosen from:
  • an antibody comprising a light chain variable domain of sequence SEQ ID No 18 or any sequence exhibiting at least 80% identity with SEQ ID No
  • an antibody comprising a light chain variable domain of sequence SEQ ID No 19 or any sequence having at least 80% identity with SEQ ID No
  • an antibody comprising a light chain variable domain of sequence SEQ ID No 20 or any sequence exhibiting at least 80% identity with SEQ ID No
  • an antibody comprising a variable domain of light chain of sequence SEQ ID No 21 or any sequence having at least 80% identity with SEQ ID No 21 and the three CDRs of heavy chains of sequences SEQ ID No 8, 2 and 3; and e) an antibody comprising a light chain variable domain of sequence SEQ ID No 22 or any sequence having at least 80% identity with SEQ ID No 22 and the three heavy chain CDRs of sequences SEQ ID No 7, 2 and 3.
  • any sequence exhibiting at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No. 18 to 22 is meant respectively the sequences exhibiting the three CDRs with light chains SEQ ID No 4, 5 and 6 and, in he
  • the antibody is chosen from:
  • an antibody comprising a light chain variable domain of sequence SEQ ID No 18 and the three heavy chain CDRs of sequence SEQ ID No 7, 2 and 3;
  • an antibody comprising a light chain variable domain of sequence SEQ ID No. 19 and the three heavy chain CDRs of sequence SEQ ID No. 7, 2 and 3;
  • an antibody comprising a light chain variable domain of sequence SEQ ID No. 20 and the three heavy chain CDRs of sequence SEQ ID No. 7, 2 and 3;
  • an antibody comprising a light chain variable domain of sequence SEQ ID No. 21 and the three heavy chain CDRs of sequence SEQ ID No. 8, 2 and 3; and e) an antibody comprising a light chain variable domain of sequence SEQ ID No 22 and the three heavy chain CDRs of sequence SEQ ID No 7, 2 and 3.
  • the antibody is an antibody chosen from:
  • an antibody comprising a heavy chain variable domain of sequence SEQ ID No 13 or any sequence having at least 80% identity with SEQ ID No
  • an antibody comprising a heavy chain variable domain of sequence SEQ ID No 14 or any sequence having at least 80% identity with SEQ ID No
  • an antibody comprising a heavy chain variable domain of sequence SEQ ID No 15 or any sequence having at least 80% identity with SEQ ID No
  • an antibody comprising a heavy chain variable domain of sequence SEQ ID No 16 or any sequence having at least 80% identity with SEQ ID No
  • the chimeric antibodies described herein can also be characterized by the constant domain and, more particularly, said chimeric antibodies can be selected or designed such as, without limitation, IgG1, IgG2, IgG3, IgM, IgA, IgD or IgE. More preferably, in the context of the present invention, said chimeric antibodies are IgG1 or IgG4.
  • the antibody is a chimeric antibody comprising the variable domains of heavy chain (VH) and of light chain (VL) as described above in the lgG1 format. More preferably, said chimeric antibody comprises a constant domain for the VH of sequence SEQ ID No 43 and a Kappa domain for the VL of sequence SEQ ID No 45.
  • the antibody is a chimeric antibody comprising the variable domains VH and VL as described above in the lgG4 format. More preferably, said chimeric antibody comprises a constant domain for the VH of sequence SEQ ID No 44 and a Kappa domain for the VL of sequence SEQ ID No 45.
  • the antibody is chosen from:
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 23 or any sequence exhibiting at least 80% identity with SEQ ID No 23 and a light chain of sequence SEQ ID No 28 or any sequence exhibiting at least 80% identity with SEQ ID No 28;
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 24 or any sequence exhibiting at least 80% identity with SEQ ID No 24 and a light chain of sequence SEQ ID No 29 or any sequence exhibiting at least 80% identity with SEQ ID No 29;
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 25 or any sequence exhibiting at least 80% identity with SEQ ID v 25 and a light chain of sequence SEQ ID v 30 or any sequence exhibiting at least 80% identity with SEQ ID No 30; d) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 26 or any sequence exhibiting at least 80% identity with SEQ ID No 26 and a light chain of sequence SEQ ID No 31 or any sequence exhibiting at least 80%% identity with SEQ ID No 31; and
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 27 or any sequence exhibiting at least 80% identity with SEQ ID No 27 and a light chain of sequence SEQ ID No 32 or any sequence exhibiting at least 80% identity with SEQ ID No 32.
  • the antibody is a humanized antibody characterized in that the constant regions of the light chain and of the heavy chain derived from the human antibody are respectively the lambda or kappa region and the gamma regions. -1, gamma-2 or gamma-4.
  • the antibody comprises a heavy chain variable domain (VH) having:
  • the antibody comprises a light chain variable domain (VL) having:
  • the antibody comprises:
  • the antibody comprises a heavy chain variable domain (VH) of sequence SEQ ID No 33 and a variable chain domain light (VL) of sequence SEQ ID No. 35.
  • VH heavy chain variable domain
  • VL variable chain domain light
  • Said humanized antibody will be called hereinafter hz208F2 (“Variant 1” or “Var. 1”).
  • the antibody comprises a heavy chain variable domain (VH) of sequence SEQ ID No 33, said sequence SEQ ID No 33 comprising at least 1 back-mutation chosen from residues 20, 34, 35, 38, 48, 50, 59, 61, 62, 70, 72, 74, 76, 77, 79, 82 and 95.
  • VH heavy chain variable domain
  • the antibody comprises a heavy chain variable domain (VH) of sequence SEQ ID No 33, said sequence SEQ ID No 33 comprising 2, 3, 4, 5, 6, 7, 8, 9, 10, 1 1, 12, 13, 14, 15, 16 or 17 back mutations chosen from residues 20, 34, 35, 38, 48, 50, 59, 61, 62, 70, 72, 74, 76, 77 , 79, 82 and 95.
  • VH heavy chain variable domain
  • the antibody comprises a light chain variable domain (VL) of sequence SEQ ID No 35, said sequence SEQ ID No 35 comprising at least 1 back-mutation chosen from residues 22, 53, 55, 65 . 71, 72, 77 and 87.
  • VL light chain variable domain
  • the antibody comprises a light chain variable domain (VL) of sequence SEQ ID No 35, said sequence of SEQ ID No 35 comprising 2, 3, 4, 5, 6, 7 or 8 back mutations chosen from residues 22, 53, 55, 65, 71, 72, 77 or 87.
  • VL light chain variable domain
  • the antibody comprises:
  • VH heavy chain variable domain
  • VL variable domain
  • the antibody comprises all the back mutations mentioned above and corresponds to an antibody comprising a heavy chain variable domain (VH) of sequence SEQ ID No 34 and a light chain variable domain (VL ) of sequence SEQ ID No. 36.
  • VH heavy chain variable domain
  • VL light chain variable domain
  • Said humanized antibody will be called hereinafter hz208F2 (“Variant 3” or “Var. 3”).
  • the antibody corresponds to an antibody comprising a heavy chain variable domain (VH) of “consensus” sequence SEQ ID No. 41 and a light chain variable domain (VL) of “consensus” sequence SEQ ID No. 42.
  • VH heavy chain variable domain
  • VL light chain variable domain
  • the humanized antibody, as a whole, will be referred to hereinafter as hz208F2 ("Variant 2" or "Var. 2").
  • the antibody is chosen from:
  • an antibody comprising a heavy chain variable domain of sequence SEQ ID No 33 or any sequence exhibiting at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No 33 and the three CDR light chains of sequences SEQ ID No 9, 5 and 11;
  • an antibody comprising a heavy chain variable domain of sequence SEQ ID No 34 or any sequence exhibiting at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No 34 and the three CDR light chains of sequences SEQ ID No 9, 5 and 11.
  • any sequence exhibiting at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No 33 or 34 is meant respectively the sequences exhibiting the three heavy chain CDRs SEQ ID No 1, 2 and 3 and, in addition, exhibiting at least 80%, preferably 85%, 90%, 95% and 98%, identity with the complete sequence SEQ ID No 33 or 34 apart from the sequences corresponding to the CDRs (i.e. SEQ ID No 1, 2 and 3).
  • the antibody is chosen from:
  • an antibody comprising a heavy chain variable domain of sequence SEQ ID No 33 or any sequence having at least 80% identity with SEQ ID No 33 and the three light chain CDRs of sequences SEQ ID No 9, 5 and 11; and b) an antibody comprising a heavy chain variable domain of sequence SEQ ID No 34 or any sequence having at least 80% identity with SEQ ID No 34 and the three light chain CDRs of sequences SEQ No NO 9, 5 and 11.
  • any sequence or by a sequence having at least 80% of a particular sequence it should be understood that said sequence has at least 80% and preferably 85%, 90%, 95% and 98% identity with the reference sequence.
  • these sequences contain CDR sequences, it is understood that the sequences exhibiting at least these CDRs must be identical to the CDRs of the reference sequence, the identities at 80%, preferably 85%, 90%, 95% and 98%, with the complete sequence having to be calculated for the remaining sequence lying outside the sequences corresponding to these CDRs.
  • the antibody is chosen from:
  • an antibody comprising a light chain variable domain of sequence SEQ ID No 35 or any sequence exhibiting at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No 35 and the three CDR heavy chains of sequences SEQ ID No 7, 2 and 3;
  • an antibody comprising a variable domain of light chain of sequence SEQ ID No 36 or any sequence exhibiting at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No 36 and the three CDR heavy chains of sequences SEQ ID No 7, 2 and 3.
  • any sequence exhibiting at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No. 35 or 36 is intended to denote the sequences exhibiting the three light chain CDRs SEQ ID No 4, 5 and 6 and, in addition, exhibiting at least 80%, preferably 85%, 90%, 95% and 98%, identity with the complete sequence SEQ ID No 35 or 36 apart from the sequences corresponding to the CDRs (namely SEQ ID No 4, 5 and 6).
  • the antibody is chosen from:
  • an antibody comprising a light chain variable domain of sequence SEQ ID No 35 or any sequence having at least 80% identity with SEQ ID No
  • humanized antibodies described here can also be characterized by the constant domain and, more particularly, said humanized antibodies can be selected in particular from lgG1, lgG2, lgG3, IgM, IgA, IgD or IgE. More preferably, in the context of the present invention, said humanized antibodies are IgG1 or IgG4.
  • the antibody is a humanized antibody comprising the variable domains VH and VL as described above in the lgG1 format. More preferably, said humanized antibody comprises a constant domain for the VH of sequence SEQ ID No 43 and a Kappa domain for the VL of sequence SEQ ID No 45.
  • the antibody is a humanized antibody comprising the variable domains VH and VL as described above in the lgG4 format. More preferably, said humanized antibody comprises a constant domain for the VH of sequence SEQ ID No 44 and a Kappa domain for the VL of sequence SEQ ID No 45.
  • the antibody is chosen from:
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 37 or any sequence exhibiting at least 80% identity with SEQ ID No 37 and a light chain of sequence SEQ ID No 39 or any sequence exhibiting at least 80% identity with SEQ ID No 39; and b) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 38 or any sequence exhibiting at least 80% identity with SEQ No 38 and a light chain of sequence SEQ ID No 40 or any sequence exhibiting at least 80 % identity with SEQ ID No 40.
  • Table 5a illustrates non-limiting examples of VH and VL sequences for variant 1 (Var. 1) and variant 3 (Var. 3) of the humanized antibody hz208F2. It also includes the consensus sequence for variant 2 (Var. 2).
  • the antibody is chosen from:
  • an antibody comprising a variable domain of heavy chain sequence chosen from SEQ ID Nos 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 and 54 or any sequence of at least 80%, preferably at least 85%, 90%, 95% and 98% identity with SEQ ID No 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 and 54; and the three CDRs of light chains of sequences SEQ ID No 9, 5 and 11;
  • an antibody comprising a variable domain of light chain sequence chosen from SEQ ID No 57 or 60 or any sequence exhibiting at least 80%, preferably at least 85%, 90%, 95% and 98% identity with SEQ ID No 57 or 60; and the three CDRs of heavy chains of sequences SEQ ID No 7, 2 and 3; and
  • an antibody comprising a variable domain of heavy chain sequence chosen from SEQ ID Nos 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 and 54 or any sequence at least 80%, preferably at least 85%, 90%, 95% and 98% identity with SEQ ID Nos 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 and 54; and a light chain variable domain chosen from SEQ ID No 57 or 60 or any sequence having at least 80%, preferably at least 85%, 90%, 95% and 98% identity with SEQ ID No 57 or 60.
  • the antibody is chosen from:
  • an antibody comprising a heavy chain of sequence SEQ ID No 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 and 54 or any sequence having at least 80% identity with SEQ ID No 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 or 54, and a light chain of sequence SEQ ID No. 57 or any sequence having at least 80% identity with SEQ ID No. 57; and
  • an antibody comprising a heavy chain of sequence SEQ ID No 56, 64, 68 and 78 or any sequence having at least 80% identity with SEQ ID No 56, 64, 68 or 78 and a light chain of sequence SEQ ID No. 60, or any sequence exhibiting at least 80% identity with SEQ ID No. 60.
  • the antibody is chosen from:
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 58 or any sequence exhibiting at least 80% identity with SEQ ID No 58 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59;
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 58 or any sequence exhibiting at least 80% identity with SEQ ID No 58 and a light chain of sequence SEQ ID No 61 or any sequence exhibiting at least 80% identity with SEQ ID No 61;
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 63 or any sequence exhibiting at least 80% identity with SEQ ID No 63 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59; d) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 65 or any sequence exhibiting at least 80% identity with SEQ ID No 65 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80%% identity with SEQ ID No 59;
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 65 or any sequence exhibiting at least 80% identity with SEQ ID No 65 and a light chain of sequence SEQ ID No 61 or any sequence exhibiting at least 80% identity with SEQ ID No 61;
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 67 or any sequence exhibiting at least 80% identity with SEQ ID No 67 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59;
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 69 or any sequence exhibiting at least 80% identity with SEQ ID No 69 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59;
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 69 or any sequence exhibiting at least 80% identity with SEQ ID No 69 and a light chain of sequence SEQ ID No 61 or any sequence exhibiting at least 80% identity with SEQ ID No 61;
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 71 or any sequence exhibiting at least 80% identity with SEQ ID No 71 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59;
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 73 or any sequence exhibiting at least 80% identity with SEQ ID No 73 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59;
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 75 or any sequence exhibiting at least 80% identity with SEQ ID No 75 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59;
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 77 or any sequence exhibiting at least 80% identity with SEQ ID No 77 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59;
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 53 or any sequence exhibiting at least 80% identity with SEQ ID No 53 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59;
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 53 or any sequence exhibiting at least 80% identity with SEQ ID No 53 and a light chain of sequence SEQ ID No 61 or any sequence exhibiting at least 80% identity with SEQ ID No 61;
  • an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 55 or any sequence exhibiting at least 80% identity with SEQ ID No 55 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59.
  • the antibody can be an antibody comprising:
  • a heavy chain of sequence selected from SEQ ID No 58, 63, 65, 67, 69, 71, 73, 75, 77, 53 and 55 or any sequence having at least 80% identity with SEQ ID No 58, 63, 65, 67, 69, 71, 73, 75, 77, 53 and 55; and
  • the antibody is chosen from:
  • a heavy chain of sequence selected from SEQ ID No 58, 63, 65, 67, 69, 71, 73, 75, 77, 53 and 55 or any sequence having at least 80% identity with SEQ ID No 58, 63, 65, 67, 69, 71, 73, 75, 77, 53 or 55;
  • Table 5b illustrates non-limiting examples of VH and VL sequences (variable domain and full length) for different variants of the humanized antibody hz208F2.
  • the antibody is an antibody produced by the hybridoma 1-4757, 1-4773, 1-4775, 1-4736 or 1-4774 deposited at the CNCM of the Institut Pasteur France. May 30, 2013, June 26, 2013, June 26, 2013, April 24, 2013 and June 26, 2013, respectively.
  • the antibody is more particularly a 208F2 antibody (eg chimeric or humanized, in particular chimeric) and more particularly a c208F2 antibody which is a monoclonal antibody (IgG1).
  • This antibody is in particular described in WO2015162291 and is characterized in that it comprises the three light chain CDRs of sequence SEQ ID Nos. 9, 5 and 11 respectively, and the three heavy chain CDRs of sequence SEQ ID Nos. 7, 2 and 3 respectively.
  • the antibody is further characterized in that it comprises a variable domain of the light chain of sequence SEQ ID No 18 and a variable domain of heavy chain of sequence SEQ ID No 13.
  • the antibody is finally characterized in that it comprises a light chain of sequence SEQ ID No 28 and a heavy chain variable domain of sequence SEQ ID No 23.
  • the c208F2 antibody and ADC-A can be obtained by any of the methods known to those skilled in the art of obtaining antibodies and ADC. They are obtained in particular by the methods described in application WO2015162291 (ADC-A preferably corresponds to the ADC named C208F2-G-13 in WO2015162291).
  • resistance is meant that the patient no longer shows a response to treatment, that is to say that there is resumption of cancer progression or stagnation.
  • treatment is meant in particular an increase in overall survival, and / or an increase in the duration of progression-free survival and / or an increase in survival without worsening and / or a decrease in recurrence and / or a decrease in the size of the tumor.
  • tumor response criteria resistance and treatment
  • RECIST criteria Engelbreviations: eisenhauer et al Eur J Cancer, 45 (2009): 228-247 or its updates.
  • the proliferative disease will be more particularly a cancer, and in particular a cancer resistant to docetaxel.
  • the cancer according to the invention may in particular be selected from cancer of the breast, colon, melanoma, lung including non-small cell lung, gastric, upper aero-digestive tract, esophagus, colorectal, gastric, glioma, esophagus, ovary, prostate, renal, thyroid, uterus, oral squamous, mesothelioma.
  • the cancer treated according to the invention will be a cancer usually treated with docetaxel, in particular gastric, prostate, lung (including non-small cell lung cancer), breast and airway cancers. -digestive superior.
  • the cancer treated according to the invention will be a cancer comprising tumor cells expressing or overexpressing all or part of the IGF-1 R protein.
  • Cancers expressing IGF-1 R may be cancers initially expressing IGF-1 R or cancers which did not initially express IGF-1 R but which started expressing it after becoming resistant to a first treatment (or more), such as resistant to docetaxel.
  • ADC-A could be administered after the development of resistance to docetaxel.
  • ADC-A can then be administered alone, after docetaxel or concomitantly with docetaxel and / or other chemotherapy.
  • the initiation of treatment with ADC-A may begin immediately after the observation of resistance, or within 1, 2, 3, 4, 5, 6, 7, or even 8 weeks or more after the observation of resistance. the occurrence of resistance, particularly before 16 weeks following the observation of the occurrence of resistance.
  • ADC-A could be administered prior to the onset of resistance to docetaxel, concomitantly with docetaxel.
  • the initiation of treatment with ADC-A can then be initiated at the same time as or after treatment with docetaxel but before the development of resistance to docetaxel.
  • compositions are administered so as to be present at the same time in the body of the patient.
  • the products can be administered simultaneously or sequentially.
  • docetaxel will depend on the severity and condition of the patient and the type of cancer to be treated. It may also vary depending on the treatments previously or concomitantly received by the patient. Generally, docetaxel is administered at a dose between 50mg / m 2 body surface area (BSA - Body area surface) and 125 mg / m 2, in particular between 75 mg / m 2 and 100 mg / m 2 every 1 to 4 weeks in particular every three weeks.
  • BSA - Body area surface body surface area
  • the number of treatment cycles (that is, the number of times the treatment is administered and the time between two doses) will depend on the patient's response and the development of resistance to docetaxel. It may in particular be between 3 and 12 cycles or more.
  • ADC-A The dosage of ADC-A will depend on the severity and condition of the patient and the type of cancer being treated. It may also vary depending on the treatments previously or concomitantly received by the patient. In general, ADC-A will be administered at a dose of between 0.5 and 3 mg / kg of patient to be treated, in particular between 0.9 and 2.5 mg / kg of patient to be treated, every 1 to 4 weeks especially every three weeks.
  • the number of cycles of treatment with ADC-A will depend in particular on the patient's response. It may in particular be between 1 and 18 cycles or more until the progression of the tumor resumes or until remission
  • the treatment according to the invention may be combined with other anti-cancer treatments before and / or concomitantly with docetaxel and / or ADC-A.
  • the anti-cancer treatment is a treatment with a molecule chosen from the group consisting of doxorubicin, cyclophosphamide, capecitabine, cisplatin, paclitaxel, carboplatin, lapatinib, pertuzimab, bevacizumab, trastuzumab, 5 -fluorouracil, anthracycline, vinorelbine, binimetinib, encorafenib and neratinib.
  • the treatment according to the invention may also be combined with other types of drugs such as corticosteroids, in particular dexamethasone or prednisone.
  • the present invention further relates to a pharmaceutical composition
  • a pharmaceutical composition comprising ADC-A and at least one pharmaceutically acceptable excipient for its use according to the invention.
  • ADC-A will be formulated so that it can be injected intravenously.
  • MCF-7 cells are obtained from ATTC (Manassas). The cells are maintained in an incubator at 5% CO2, 90% humidity and 37 ° C in standard cell culture medium, as recommended by the supplier.
  • the 208F2 antibody is produced as described in application WO2015162291. Briefly, the anti-IGF-1 R antibody, humanized c208F2 (hz208F2 (4)) is generated using hybridoma technology. Balb / c mice are immunized with the recombinant human protein IGF-1 R (rhlGF-1 R) (R&D systems) in the presence of Freund's adjuvant. The spleens are fused with the myeloma fusion partner SP2 / 0. After limiting dilution cloning, binding and internalization of the antibody to MCF-7 cells is confirmed and the isotype determined.
  • the binding specificity is verified by ELISA on rhlGF-1 R, the recombinant human insulin receptor (rhIR) and murine IGF-1 R (mlGF-1 R) (R&D systems).
  • the m208F2 antibody is then humanized by complementarity determining regions (CDRs) grafting and expressed in Chinese hamster ovary cells for complete pharmacological characterization.
  • ADC-A is produced as described in application WO2015162291 (ADC-A corresponds to the ADC named C208F2-G-13 of WO2015162291).
  • a slight reduction of mAb 208F2 (hz208F2-4) and coupling to the payload linker is carried out as described previously (Sun et al. Bioconjug. Chem 2005; 16: 1282-90, Wagner-Rousset et al Mabs 2014; 6: 173- 84). Briefly, to target a DAR of 4, hz208F2-4 was reduced with 2.5 molar equivalents of tris (2-carboxyethyl) phosphine (TCEP).
  • TCEP (2-carboxyethyl) phosphine
  • linker-payload (G-13).
  • ADC-A is concentrated to 5 mg / mL (in buffer in 25 mM histidine pH 6.5, 150 mM NaCl and 6% sucrose). Tween 80 was then added to obtain a final concentration of 0.005% (v / v).
  • the product is finally filtered through a Stericup filter (GP Express PLUS Membrane, 0.22pm, Polyethersulfone, Millipore) and stored at 4 ° C.
  • mice are randomized, and treatment is initiated when the tumors reach a size of approximately 150 mm 3 .
  • the tumor volume (length c width c height c 0.52) is measured at least twice a week and the therapeutic response is defined using the criteria for evaluating the response of solid tumors (RECIST).
  • mice bearing MCF-7 tumors are injected intravenously with docetaxel, 9 mg / kg twice weekly, with a total of 5 injections.
  • group 1 receives 9 mg / kg of docetaxel every 2 weeks and group 2 receives a single injection of ADC-A of 3 mg / kg.
  • T the volume of the tumor in the treated group
  • DT the volume of the tumor in the treated group on the day of the study minus the volume of the tumor in the treated group on the initial day of administration
  • Tinitial the volume of the tumor in the treated group on the initial day of administration.
  • PR is defined as a decrease in tumor size> 30%. Lack of tumor growth, or a slight decrease ( ⁇ 30%), or slight increase ( ⁇ 20%) in tumor size is defined as stable disease (SD), and an absence of palpable tumor mass is defined as a complete regression (CR).
  • ADC-A In order to assess the therapeutic potential of ADC-A in breast cancer, the effect of ADC-A administration was studied in a mouse model grafted with MCF-7 cells after the appearance of resistance. with docetaxel. After 70 days, the tumors became resistant to docetaxel and relapsed (Fig. 1). Administration of a single dose of ADC-A of 3 mg / kg in mice with tumors resistant to docetaxel induces a strong and significant inhibition of tumor growth (P 0.05) (Fig. 1), CR is observed in 1 mouse and RP in 3 out of 5 mice. ADC-A and docetaxel exhibits a synergistic effect.
  • ADC-A is a good treatment alone or in combination with docetaxel for the treatment of tumors resistant to docetaxel. This is all the more surprising given that the payload used has a similar mechanism of action (action on tubulin) to taxanes and therefore to docetaxel.

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Abstract

The present invention relates to an ADC having the following formula (I) in which Ab is an anti-IGF1R antibody characterized in that it comprises light chain CDRs of sequences SEQ ID Nos. 9, 5 and 11, respectively, and heavy chain CDRs of sequences SEQ ID Nos. 7, 2 and 3, respectively, and n is between 1 and 12, for use in the treatment of proliferative diseases, such as cancer, characterized in that the ADC is administered concomitantly with or subsequent to docetaxel.

Description

l l
ADC pour un traitement concomitant ou postérieur au docétaxel ADC for concomitant or post-docetaxel treatment
La présente invention porte sur l’utilisation d’un ADC anti-IGF1 R (ADC-A) pour le traitement de maladies prolifératives, telles que le cancer, caractérisée en ce que ADC-A est administré de façon concomitante ou postérieurement au docétaxel. The present invention relates to the use of an anti-IGF1 R ADC (ADC-A) for the treatment of proliferative diseases, such as cancer, characterized in that ADC-A is administered concomitantly or subsequently to docetaxel.
Le traitement maladies hyperprolifératives, telles que le cancer, constitue un réel challenge de santé public. Il s’agit, bien entendu, de trouver en premier lieu des médicaments anti-tumoraux efficaces. Mais il s’agit aussi de prévoir des solutions à long terme en cas d’apparition de résistance, phénomène fréquent, à ces premiers traitements. The treatment of hyperproliferative diseases, such as cancer, constitutes a real public health challenge. The first thing, of course, is to find effective anti-tumor drugs. But it is also a matter of providing long-term solutions in the event of the appearance of resistance, a frequent phenomenon, to these first treatments.
Le docétaxel est un diterpène utilisé comme médicament anti-cancéreux qui agit sur les microtubules des cellules cancéreuses et entraîne un blocage de la mitose. L’efficacité du docétaxel a été prouvé dans un assez grand nombre de tumeurs notamment cancer du sein, cancer du poumon, cancer de la prostate. Cependant un grand nombre de patients développe au fil du temps une résistance au docétaxel aboutissant à l’échec du traitement. Docetaxel is a diterpene used as an anti-cancer medicine that acts on the microtubules of cancer cells and results in the blocking of mitosis. The efficacy of docetaxel has been proven in quite a number of tumors including breast cancer, lung cancer, prostate cancer. However, over time a large number of patients develop resistance to docetaxel leading to treatment failure.
Le récepteur du facteur de croissance 1 analogue à l'insuline appelé IGF-1 R (ou IGF1 R) est un récepteur à activité tyrosine kinase ayant une homologie de 70 % avec le récepteur à l'insuline IR. IGF-IR est une glycoprotéine de poids moléculaire d'environ 350 000. Il s'agit d'un récepteur hétérotétramère dont chaque moitié - liée par des ponts disulfure - est composée d'une sous-unité extracellulaire a et d'une sous- unité transmembranaire b. IGF-IR lie IGF1 et IGF2 avec une affinité très élevée (Kd #1 nM) et est capable de se lier à l'insuline avec une affinité 100 à 1000 fois inférieure. The insulin-like growth factor 1 receptor referred to as IGF-1 R (or IGF1 R) is a receptor with tyrosine kinase activity having 70% homology to the insulin receptor IR. IGF-IR is a glycoprotein with a molecular weight of approximately 350,000. It is a heterotetrameric receptor in which each half - linked by disulfide bonds - is composed of an extracellular α subunit and a subunit. transmembrane unit b. IGF-IR binds IGF1 and IGF2 with very high affinity (Kd # 1 nM) and is able to bind to insulin with 100 to 1000 times lower affinity.
Des protéines tyrosine kinase cytoplasmiques sont activées par la liaison du ligand au domaine extracellulaire d’IGF-1 R. L'activation de ces kinases entraîne à son tour l’activation de différents substrats intracellulaires, dont IRS-1 , IRS-2, She et Grb 10. Les protéines 1RS interviennent, par l'activation de nombreux effecteurs en aval, dans de nombreuses voies induisant la croissance et la différenciation cellulaires. Il semble, en outre, que la voie principalement impliquée dans la protection contre l'apoptose soit la voie des phosphatidyl-inositol 3-kinases (PI3-kinases). Cytoplasmic protein tyrosine kinases are activated by ligand binding to the extracellular domain of IGF-1 R. Activation of these kinases in turn results in the activation of various intracellular substrates, including IRS-1, IRS-2, She and Grb 10. The 1RS proteins are involved, through the activation of numerous downstream effectors, in numerous pathways inducing cell growth and differentiation. It seems, moreover, that the pathway mainly involved in the protection against apoptosis is the path of phosphatidyl-inositol 3-kinases (PI3-kinases).
Le rôle du système IGF dans la cancérogenèse a fait l'objet de recherches intensives au cours des dix dernières années. En effet, il est bien établi qu’une activation de l'IGF-IR conduit, dans une grande variété de cellules, à une croissance anormale des cellules indépendante et à la formation de tumeurs. IGF-IR est ainsi exprimé dans une grande variété de tumeurs et de lignées tumorales. The role of the IGF system in carcinogenesis has been the subject of intensive research over the past decade. Indeed, it is well established that a Activation of IGF-IR leads, in a wide variety of cells, to independent abnormal cell growth and tumor formation. IGF-IR is thus expressed in a wide variety of tumors and tumor lines.
Afin de traiter ce type de cancer, des thérapies ciblées visant IGF1 R ont été mises au point. Il a ainsi été prouvé que l’utilisation d’ADC (antibody-drug conjugate) ciblant IGF-1 R permet de réduire, voire d’abolir la croissance tumorale. De tels ADC ont notamment été décrits dans la demande de brevet WO2015162291 en particulier l’ADC décrit ci-après et nommé ADC-A. In order to treat this type of cancer, targeted therapies targeting IGF1 R have been developed. It has thus been proved that the use of ADC (antibody-drug conjugate) targeting IGF-1 R can reduce or even abolish tumor growth. Such ADCs have in particular been described in patent application WO2015162291, in particular the ADC described below and named ADC-A.
Il existe un réel besoin de traitement efficace des maladies hyper-prolifératives. II est par ailleurs nécessaire d’identifier des combinaisons de thérapies permettant d’échapper au phénomène d’apparition de résistance au sein des tumeurs. There is a real need for an effective treatment of hyperproliferative diseases. It is also necessary to identify combinations of therapies that make it possible to avoid the phenomenon of the appearance of resistance within tumors.
De façon surprenante, la présente invention a permis de montrer que l’utilisation d’un ADC anti-IGF1 R en combinaison avec le docétaxel permet d’obtenir un effet synergique dans le traitement des tumeurs. De façon toute aussi surprenante il a été montré que l’utilisation d’un ADC anti-IGF1 R permet de traiter les tumeurs devenues résistantes après un traitement au docétaxel. Surprisingly, the present invention has made it possible to show that the use of an anti-IGF1 R ADC in combination with docetaxel makes it possible to obtain a synergistic effect in the treatment of tumors. Equally surprisingly, it has been shown that the use of an anti-IGF1 R ADC can treat tumors that have become resistant after treatment with docetaxel.
Légende de la Figure : Figure legend:
FIG 1 : Evolution du volume tumoral moyen en mm3 en fonction du temps en jours chez des souris porteuses d’une tumeur MCF-7 d’environ 150 mm3 après A. Traitement par du docétaxel à 9mg/kg une fois toutes les deux semaines pendant 5 cycles (les trois courbes confondues correspondent à trois séries de 5 souris traitées de façon identique et au même moment) et B. Traitement des souris rendues résistantes au docétaxel au jour 70 par : groupe 1 , du docétaxel 9 mg/kg toutes les deux semaines (courbe points ronds) et ; groupe 2, une injection de ADC-A à 3 mg/kg (courbe points triangles). FIG 1: Evolution of the average tumor volume in mm 3 as a function of time in days in mice bearing an MCF-7 tumor of approximately 150 mm 3 after A. Treatment with docetaxel at 9 mg / kg once every two weeks for 5 cycles (the three curves combined correspond to three series of 5 mice treated identically and at the same time) and B. Treatment of mice made resistant to docetaxel on day 70 with: group 1, docetaxel 9 mg / kg all the two weeks (round point curve) and; group 2, an injection of ADC-A at 3 mg / kg (curve points triangles).
La présente invention a ainsi pour objet un ADC anti-IGF1 R (ADC-A) pour son utilisation dans le traitement de maladies prolifératives, telles que le cancer, caractérisé en ce que ADC-A est administré de façon concomitante ou postérieurement à du docétaxel. La présente invention a également pour objet l’utilisation d’un ADC anti-IGF1 R (ADC-A) pour le traitement de maladies prolifératives, telles que le cancer, caractérisée en ce que ADC-A est administré de façon concomitante ou postérieurement à du docétaxel. A subject of the present invention is thus an anti-IGF1 R ADC (ADC-A) for its use in the treatment of proliferative diseases, such as cancer, characterized in that ADC-A is administered concomitantly or subsequently to docetaxel . A subject of the present invention is also the use of an anti-IGF1 R ADC (ADC-A) for the treatment of proliferative diseases, such as cancer, characterized in that ADC-A is administered concomitantly or subsequently to docetaxel.
La présente invention a également pour objet l’utilisation d’un ADC anti-IGF1 R The present invention also relates to the use of an anti-IGF1 R ADC
(ADC-A) pour la préparation d’un médicament destiné au traitement de maladies prolifératives, telles que le cancer, caractérisée en ce que ADC-A est administré de façon concomitante ou postérieurement à du docétaxel. (ADC-A) for the preparation of a medicament for the treatment of proliferative diseases, such as cancer, characterized in that ADC-A is administered concomitantly or subsequently with docetaxel.
La présente invention a également pour objet une méthode de traitement d’une maladie proliférative, telle que le cancer, comprenant l’administration à un patient en ayant besoin d’une quantité efficace d’un ADC anti-IGF1 R (ADC-A) et de docétaxel, caractérisée en ce que ADC-A est administré de façon concomitante ou postérieurement au docétaxel. The present invention also relates to a method of treating a proliferative disease, such as cancer, comprising administering to a patient in need an effective amount of an anti-IGF1 R ADC (ADC-A). and docetaxel, characterized in that ADC-A is administered concomitantly or subsequent to docetaxel.
Docétaxel Docetaxel
Par docétaxel, selon l’invention, on entend le composé de formule suivante : By docetaxel, according to the invention, is meant the compound of the following formula:
ainsi que ses sels et solvatés pharmaceutiquement acceptables, notamment son trihydrate. as well as its pharmaceutically acceptable salts and solvates, in particular its trihydrate.
Le docétaxel est notamment vendu sous le nom de marque Taxotere®. Docetaxel is notably sold under the brand name Taxotere®.
Dans la présente invention, on entend désigner par « pharmaceutiquement acceptable » ce qui est utile dans la préparation d'une composition pharmaceutique qui est généralement sûr, non toxique et ni biologiquement ni autrement non souhaitable et qui est acceptable pour une utilisation vétérinaire de même que pharmaceutique humaine. On entend désigner par « sel ou solvaté pharmaceutiquement acceptable » d’un composé, un sel ou solvaté qui est pharmaceutiquement acceptable, comme défini ici, et qui possède l’activité pharmacologique souhaitée du composé parent. In the present invention, by "pharmaceutically acceptable" is meant that which is useful in the preparation of a pharmaceutical composition which is generally safe, non-toxic and neither biologically nor otherwise undesirable and which is acceptable for veterinary use as well as human pharmaceutical. By "pharmaceutically acceptable salt or solvate" of a compound is meant a salt or solvate which is pharmaceutically acceptable, as defined herein, and which has the desired pharmacological activity of the parent compound.
Les sels pharmaceutiquement acceptables comprennent notamment : Pharmaceutically acceptable salts include in particular:
(1 ) les sels d’addition d’acide pharmaceutiquement acceptable formés avec des acides inorganiques pharmaceutiquement acceptables tels que l’acide chlorhydrique, l’acide bromhydrique, l’acide sulfurique, l’acide nitrique, l’acide phosphorique et similaires ; ou formés avec des acides organiques pharmaceutiquement acceptables tels que l’acide formique, l’acide acétique, l’acide benzènesulfonique, l’acide benzoïque, l’acide camphresulfonique, l’acide citrique, l’acide éthane-sulfonique, l’acide fumarique, l’acide glucoheptonique, l’acide gluconique, l’acide glutamique, l’acide glycolique, l’acide hydroxynaphtoïque, l'acide 2-hydroxyéthanesulfonique, l’acide lactique, l’acide maléique, l’acide malique, l’acide mandélique, l’acide méthanesulfonique, l’acide muconique, l’acide 2-naphtalènesulfonique, l’acide propionique, l’acide salicylique, l’acide succinique, l’acide dibenzoyl-L-tartrique, l’acide tartrique, l’acide p-toluènesulfonique, l’acide triméthylacétique, l’acide trifluoroacétique et similaires, et (1) the pharmaceutically acceptable acid addition salts formed with pharmaceutically acceptable inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid and the like; or formed with pharmaceutically acceptable organic acids such as formic acid, acetic acid, benzenesulfonic acid, benzoic acid, camphorsulfonic acid, citric acid, ethanesulfonic acid, fumaric acid, glucoheptonic acid, gluconic acid, glutamic acid, glycolic acid, hydroxynaphthoic acid, 2-hydroxyethanesulfonic acid, lactic acid, maleic acid, malic acid, l 'mandelic acid, methanesulfonic acid, muconic acid, 2-naphthalenesulfonic acid, propionic acid, salicylic acid, succinic acid, dibenzoyl-L-tartaric acid, tartaric acid, p-toluenesulfonic acid, trimethylacetic acid, trifluoroacetic acid and the like, and
(2) les sels d’addition de base pharmaceutiquement acceptable formés lorsqu’un proton acide présent dans le composé parent est soit remplacé par un ion métallique, par exemple un ion de métal alcalin, un ion de métal alcalino-terreux ou un ion d'aluminium ; soit coordonné avec une base organique pharmaceutiquement acceptable telle que la diéthanolamine, l’éthanolamine, N-méthylglucamine, la triéthanolamine, la trométhamine et similaires ; ou avec une base inorganique pharmaceutiquement acceptable telle que l’hydroxyde d’aluminium, l’hydroxyde de calcium, l’hydroxyde de potassium, le carbonate de sodium, l’hydroxyde de sodium et similaires. (2) the pharmaceutically acceptable base addition salts formed when an acidic proton present in the parent compound is either replaced by a metal ion, for example an alkali metal ion, an alkaline earth ion or a d ion. aluminum; is coordinated with a pharmaceutically acceptable organic base such as diethanolamine, ethanolamine, N-methylglucamine, triethanolamine, tromethamine and the like; or with a pharmaceutically acceptable inorganic base such as aluminum hydroxide, calcium hydroxide, potassium hydroxide, sodium carbonate, sodium hydroxide and the like.
Des solvatés acceptables pour l’utilisation pharmaceutique des composés selon la présente invention incluent des solvatés conventionnels tels que ceux formés, durant la dernière étape du procédé de préparation des composés selon l’invention, avec le(s) solvant(s) de réaction. A titre d’exemple, il peut être fait mention des solvatés formés avec l’eau (appelés communément hydrates) ou avec l’éthanol. Il peut s’agir par un exemple d’un trihydrate. ADC-A Solvates acceptable for the pharmaceutical use of the compounds according to the present invention include conventional solvates such as those formed, during the last step of the process for preparing the compounds according to the invention, with the reaction solvent (s). By way of example, mention may be made of solvates formed with water (commonly called hydrates) or with ethanol. It may be, for example, a trihydrate. ADC-A
ADC-A est un ADC anti-IGF1 R de formule suivante ADC-A is an anti-IGF1 R ADC of the following formula
dans laquelle Ab est un anticorps anti-IGF1 R comprenant les trois CDR (régions complémentaires déterminantes - complementarity determining régions en anglais) de chaînes lourdes de séquences SEQ ID No 1 , 2 et 3 et les trois CDR de chaîne légère de séquences SEQ ID No 4, 5 et 6, et n est compris entre 1 et 12, notamment est égale à 2 ou 4. in which Ab is an anti-IGF1 R antibody comprising the three CDRs (complementarity determining regions) of heavy chains of sequences SEQ ID No 1, 2 and 3 and the three CDRs of light chain of sequences SEQ ID No 4, 5 and 6, and n is between 1 and 12, in particular is equal to 2 or 4.
Les termes « anticorps », « ab », « Ab », « Mab » ou « immunoglobuline » sont utilisés indifféremment dans le sens le plus large et comprennent les anticorps monoclonaux, les anticorps isolés, modifiés ou recombinants (par exemple, les anticorps monoclonaux complets ou intacts), les anticorps polyclonaux, les anticorps multivalents ou des anticorps multispécifiques (par exemple des anticorps bispécifiques) ainsi que les fragments d’anticorps de ceux-ci, pour autant qu’ils présentent l’activité biologique souhaitée, en particulier les fragments de ceux-ci se liant à l’antigène. Il s’agit plus particulièrement d’anticorps monoclonaux ou éventuellement de fragments de ceux-ci se liant à l’antigène. The terms "antibody", "ab", "Ab", "Mab" or "immunoglobulin" are used interchangeably in the broadest sense and include monoclonal antibodies, isolated, modified or recombinant antibodies (for example, monoclonal antibodies complete or intact), polyclonal antibodies, multivalent antibodies or multispecific antibodies (e.g. bispecific antibodies) as well as antibody fragments thereof, provided that they exhibit the desired biological activity, in particular the fragments thereof binding to the antigen. They are more particularly monoclonal antibodies or possibly fragments thereof which bind to the antigen.
Le terme « fragment se liant à l'antigène » d'un anticorps selon l'invention est destiné à indiquer tout peptide, polypeptide ou protéine conservant l'aptitude à se lier à la cible (également appelée généralement antigène) de l'anticorps. The term “antigen-binding fragment” of an antibody according to the invention is intended to indicate any peptide, polypeptide or protein which retains the ability to bind to the target (also generally called antigen) of the antibody.
Tel qu'utilisé dans la présente description, l'expression « anticorps anti-IGF-1 R » désigne un anticorps capable de se lier à IGF-1 R, plus particulièrement à un épitope localisé dans IGF-1 R, de préférence le domaine extracellulaire de l’IGF-1 R, plus préférablement l'IGF-1 R humain (SEQ ID No 50) et encore plus préférablement le domaine extracellulaire de l'IGF-1 R humain (SEQ ID No 51), et encore plus préférablement la partie N-terminale du domaine extracellulaire de l'IGF-1 R humain (SEQ ID No 52), ou l'une quelconque de ses séquences variantes naturelles. As used in the present description, the expression “anti-IGF-1 R antibody” denotes an antibody capable of binding to IGF-1 R, more particularly to an epitope located in IGF-1 R, preferably the domain extracellular IGF-1 R, more preferably human IGF-1 R (SEQ ID No 50) and still more preferably the extracellular domain of human IGF-1 R (SEQ ID No 51), and still more preferably the N-terminal part of the extracellular domain of human IGF-1R (SEQ ID No 52), or any of its naturally occurring variant sequences.
Selon un mode de réalisation particulier de l'invention, l'anticorps selon l’invention comprend les trois CDR de chaînes lourdes comprenant ou consistant en les séquences SEQ ID No 1 , 2 et 3, ou toute séquence présentant au moins 80%, de préférence 85%, 90%, 95% et 98% d'identité avec SEQ ID No 1 , 2 ou 3; et les trois CDR de chaînes légères comprenant ou consistant en les séquences SEQ ID No 4, 5 et 6, ou toute séquence présentant au moins 80%, de préférence 85%, 90%, 95% et 98% d'identité avec la SEQ ID No 4, 5 ou 6. According to a particular embodiment of the invention, the antibody according to the invention comprises the three CDRs of heavy chains comprising or consisting of the sequences SEQ ID No 1, 2 and 3, or any sequence having at least 80%, of preferably 85%, 90%, 95% and 98% identity with SEQ ID No 1, 2 or 3; and the three CDRs of light chains comprising or consisting of the sequences SEQ ID No 4, 5 and 6, or any sequence having at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No 4, 5 or 6.
Les pourcentages d’identité auxquels il est fait référence dans le cadre de l’exposé de la présente invention sont déterminés sur la base d’un alignement global des séquences à comparer, c’est-à-dire sur un alignement des séquences prises dans leur intégralité sur toute la longueur en utilisant tout algorithme bien connu de l'homme du métier tel que l’algorithme de Needleman et Wunsch-1970. Cette comparaison de séquences peut être effectuée à l'aide de tout logiciel bien connu de l'homme du métier : par exemple le logiciel needle en utilisant le paramètre « Gap open » égal à 10,0, le paramètre « Gap extend » égal à 0,5 et une matrice « Blosum 62 ». Le logiciel needle est par exemple disponible sur le site internet ebi.ac.uk world wide sous la dénomination « Align ». The percentages of identity to which reference is made in the context of the disclosure of the present invention are determined on the basis of an overall alignment of the sequences to be compared, that is to say on an alignment of the sequences taken in their entirety over the entire length using any algorithm well known to those skilled in the art such as the algorithm of Needleman and Wunsch-1970. This sequence comparison can be performed using any software well known to those skilled in the art: for example the needle software using the “Gap open” parameter equal to 10.0, the “Gap extend” parameter equal to 0.5 and a “Blosum 62” matrix. The needle software is for example available on the ebi.ac.uk world wide website under the name “Align”.
Lorsque l’anticorps selon l’invention possède une séquence d’acides aminés qui n’est pas 100% identique à la séquence de référence mais qui possède au moins 80%, de préférence 85%, 90%, 95% et 98% d’identité avec une telle séquence de référence, elle peut présenter des insertions, délétions ou substitutions par rapport à la séquence de référence. Lorsqu’il s’agit de substitutions, la substitution est de préférence réalisée par un acide aminé « équivalent », c'est-à-dire tout acide aminé dont la structure est proche de celle de l’acide aminé d’origine et est donc peu probable de modifier les activités biologiques de l’anticorps. Des exemples de telles substitutions sont présentés dans le tableau suivant : When the antibody according to the invention has an amino acid sequence which is not 100% identical to the reference sequence but which has at least 80%, preferably 85%, 90%, 95% and 98% d 'identity with such a reference sequence, it may present insertions, deletions or substitutions with respect to the reference sequence. When it comes to substitutions, the substitution is preferably carried out by an “equivalent” amino acid, that is to say any amino acid whose structure is close to that of the original amino acid and is therefore unlikely to modify the biological activities of the antibody. Examples of such substitutions are shown in the following table:
Le tableau 1 ci-dessous illustre les séquences des CDR pour les anticorps préférés : Table 1 below illustrates the CDR sequences for the preferred antibodies:
Tableau 1 Table 1
Selon un aspect spécifique, l'anticorps est un anticorps murin caractérisé en ce qu'il comprend également des régions constantes de chaîne légère et de chaîne lourde dérivées d'un anticorps d'une espèce hétérologue chez la souris, notamment l'homme. According to a specific aspect, the antibody is a murine antibody characterized in that it also comprises constant regions of light chain and of heavy chain derived from an antibody of a heterologous species in mice, in particular humans.
Selon un aspect spécifique de l’invention, l'anticorps est un anticorps chimérique (c) caractérisé en ce qu'il comprend également des régions constantes de chaînes légères et lourdes dérivées d'un anticorps d'une espèce hétérologue avec la souris, notamment humaine. According to a specific aspect of the invention, the antibody is a chimeric antibody (c) characterized in that it also comprises constant regions of light and heavy chains derived from an antibody of a species heterologous with the mouse, in particular human.
Un anticorps chimérique est un anticorps contenant une région variable naturelle (chaîne légère et chaîne lourde) dérivée d'un anticorps d'une espèce donnée en combinaison avec des régions constantes de la chaîne légère et la chaîne lourde d'un anticorps d'une espèce hétérologue à ladite espèce donnée. Selon un mode de réalisation de l'invention, l'anticorps est choisi parmi : A chimeric antibody is an antibody containing a natural variable region (light chain and heavy chain) derived from an antibody of a given species in combination with constant regions of the light chain and the heavy chain of an antibody of a species heterologous to said given species. According to one embodiment of the invention, the antibody is chosen from:
a) un anticorps comprenant les trois CDR à chaînes lourdes de séquences SEQ ID No 7, 2 et 3 et les trois CDR à chaînes légères de séquences SEQ ID No 9, 5 et 11 ; b) un anticorps comprenant les trois CDR à chaînes lourdes de séquences SEQ ID No 7, 2 et 3 et les trois CDR à chaînes légères de séquences SEQ ID No 10, 5 et 11 ; c) un anticorps comprenant les trois CDR à chaînes lourdes de séquences SEQ ID Noa) an antibody comprising the three CDRs with heavy chains of sequences SEQ ID No 7, 2 and 3 and the three CDRs with light chains of sequences SEQ ID No 9, 5 and 11; b) an antibody comprising the three CDRs with heavy chains of sequences SEQ ID No 7, 2 and 3 and the three CDRs with light chains of sequences SEQ ID No 10, 5 and 11; c) an antibody comprising the three CDRs with heavy chains of sequences SEQ ID No
7, 2 et 3 et les trois CDR à chaînes légères de séquences SEQ ID No 9, 5 et 12 ; et d) un anticorps comprenant les trois CDR à chaînes lourdes de séquences SEQ ID No7, 2 and 3 and the three CDRs with light chains of sequences SEQ ID Nos. 9, 5 and 12; and d) an antibody comprising the three CDRs with heavy chains of sequences SEQ ID No
8, 2 et 3 et les trois CDR à chaînes légères de séquences SEQ I D No 9, 5 et 11. 8, 2 and 3 and the three CDRs with light chains of sequences SEQ I D No 9, 5 and 11.
Dans un mode de réalisation préféré mais non limitatif, l'anticorps est choisi parmi : In a preferred but non-limiting embodiment, the antibody is chosen from:
a) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 13 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID Noa) an antibody comprising a heavy chain variable domain of sequence SEQ ID No 13 or any sequence having at least 80% identity with SEQ ID No
13 et les trois CDR de chaîne légère de séquences SEQ ID No 9, 5 et 11 ; 13 and the three light chain CDRs of sequences SEQ ID Nos. 9, 5 and 11;
b) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 14 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID Nob) an antibody comprising a heavy chain variable domain of sequence SEQ ID No 14 or any sequence having at least 80% identity with SEQ ID No
14 et les trois CDR de chaîne légère de séquences SEQ ID No 10, 5 et 11 ; 14 and the three light chain CDRs of sequences SEQ ID Nos 10, 5 and 11;
c) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 15 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 15 et les trois CDR de chaîne légère de séquences SEQ ID No 9, 5 et 12 ; c) an antibody comprising a heavy chain variable domain of sequence SEQ ID No 15 or any sequence having at least 80% identity with SEQ ID No 15 and the three light chain CDRs of sequences SEQ ID No 9, 5 and 12;
d) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 16 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID Nod) an antibody comprising a heavy chain variable domain of sequence SEQ ID No 16 or any sequence having at least 80% identity with SEQ ID No
16 et les trois CDR de chaîne légère de séquences SEQ ID No 9, 5 et 11 ; et e) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 17 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No16 and the three light chain CDRs of sequences SEQ ID Nos. 9, 5 and 11; and e) an antibody comprising a heavy chain variable domain of sequence SEQ ID No 17 or any sequence having at least 80% identity with SEQ ID No
17 et les trois CDR de chaîne légère de séquences SEQ ID No 9, 5 et 12. 17 and the three light chain CDRs of sequences SEQ ID No 9, 5 and 12.
Par « toute séquence présentant au moins 80%, de préférence 85%, 90%, 95% et 98% d'identité avec SEQ ID No 13 à 17 », on entend respectivement les séquences présentant les trois CDR à chaînes lourdes SEQ ID No 1 , 2 et 3 et, en outre, présentant au moins 80%, de préférence 85%, 90%, 95% et 98%, d’identité avec la séquence complète SEQ ID No 13 à 17 en dehors des séquences correspondant aux CDR (c'est- à-dire SEQ ID No 1 , 2 et 3). Selon un mode de réalisation de l'invention, l'anticorps est choisi parmi : By “any sequence exhibiting at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No 13 to 17”, is meant respectively the sequences exhibiting the three CDRs with heavy chains SEQ ID No 1, 2 and 3 and, in addition, exhibiting at least 80%, preferably 85%, 90%, 95% and 98%, identity with the complete sequence SEQ ID No 13 to 17 apart from the sequences corresponding to the CDRs (i.e. SEQ ID No 1, 2 and 3). According to one embodiment of the invention, the antibody is chosen from:
a) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 13 et les trois CDR de chaîne légère de séquence SEQ ID No 9, 5 et 11 ; b) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 14 et les trois CDR de chaîne légère de séquence SEQ ID No 10, 5 et 11 ; c) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 15 et les trois CDR de chaîne légère de séquence SEQ ID No 9, 5 et 12 ; d) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 16 et les trois CDR de chaîne légère de séquence SEQ ID No 9, 5 et 11 ; et e) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 17 et les trois CDR de chaîne légère de séquence SEQ ID No 9, 5 et 12. a) an antibody comprising a heavy chain variable domain of sequence SEQ ID No. 13 and the three light chain CDRs of sequence SEQ ID No. 9, 5 and 11; b) an antibody comprising a heavy chain variable domain of sequence SEQ ID No. 14 and the three light chain CDRs of sequence SEQ ID No. 10, 5 and 11; c) an antibody comprising a heavy chain variable domain of sequence SEQ ID No. 15 and the three light chain CDRs of sequence SEQ ID No. 9, 5 and 12; d) an antibody comprising a heavy chain variable domain of sequence SEQ ID No. 16 and the three light chain CDRs of sequence SEQ ID No. 9, 5 and 11; and e) an antibody comprising a heavy chain variable domain of sequence SEQ ID No 17 and the three light chain CDRs of sequence SEQ ID No 9, 5 and 12.
Dans un autre mode de réalisation préféré mais non limitatif, l'anticorps est choisi parmi : In another preferred but non-limiting embodiment, the antibody is chosen from:
a) un anticorps comprenant un domaine variable de chaîne légère de séquence SEQ ID No 18 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID Noa) an antibody comprising a light chain variable domain of sequence SEQ ID No 18 or any sequence exhibiting at least 80% identity with SEQ ID No
18 et les trois CDR de chaînes lourdes de séquences SEQ ID No 7, 2 et 3 ; 18 and the three CDRs of heavy chains of sequences SEQ ID No 7, 2 and 3;
b) un anticorps comprenant un domaine variable de chaîne légère de séquence SEQ ID No 19 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID Nob) an antibody comprising a light chain variable domain of sequence SEQ ID No 19 or any sequence having at least 80% identity with SEQ ID No
19 et les trois CDR de chaînes lourdes de séquences SEQ ID No 7, 2 et 3 ; 19 and the three CDRs of heavy chains of sequences SEQ ID No 7, 2 and 3;
c) un anticorps comprenant un domaine variable de chaîne légère de séquence SEQ ID No 20 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID Noc) an antibody comprising a light chain variable domain of sequence SEQ ID No 20 or any sequence exhibiting at least 80% identity with SEQ ID No
20 et les trois CDR de chaîne lourde de séquences SEQ ID No 7, 2 et 3 ; And the three heavy chain CDRs of sequences SEQ ID Nos. 7, 2 and 3;
d) un anticorps comprenant un domaine variable de chaîne légère de séquence SEQ ID No 21 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 21 et les trois CDR de chaînes lourdes de séquences SEQ ID No 8, 2 et 3 ; et e) un anticorps comprenant un domaine variable de chaîne légère de séquence SEQ ID No 22 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 22 et les trois CDR de chaîne lourde des séquences SEQ ID No 7, 2 et 3. d) an antibody comprising a variable domain of light chain of sequence SEQ ID No 21 or any sequence having at least 80% identity with SEQ ID No 21 and the three CDRs of heavy chains of sequences SEQ ID No 8, 2 and 3; and e) an antibody comprising a light chain variable domain of sequence SEQ ID No 22 or any sequence having at least 80% identity with SEQ ID No 22 and the three heavy chain CDRs of sequences SEQ ID No 7, 2 and 3.
Par « toute séquence présentant au moins 80%, de préférence 85%, 90%, 95% et 98% d'identité avec la SEQ ID No 18 à 22 », on entend respectivement les séquences présentant les trois CDR à chaînes légères SEQ ID No 4, 5 et 6 et, en il By “any sequence exhibiting at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No. 18 to 22”, is meant respectively the sequences exhibiting the three CDRs with light chains SEQ ID No 4, 5 and 6 and, in he
outre, présentant au moins 80%, de préférence 85%, 90%, 95% et 98%, d’identité avec la séquence complète SEQ ID No 18 à 22 en dehors des séquences correspondant aux CDR (c'est-à-dire SEQ ID No 4, 5 et 6). furthermore, exhibiting at least 80%, preferably 85%, 90%, 95% and 98%, identity with the complete sequence SEQ ID No 18 to 22 apart from the sequences corresponding to the CDRs (that is to say SEQ ID No 4, 5 and 6).
Selon un mode de réalisation de l'invention, l'anticorps est choisi parmi : According to one embodiment of the invention, the antibody is chosen from:
a) un anticorps comprenant un domaine variable de chaîne légère de séquence SEQ ID No 18 et les trois CDR de chaîne lourde de séquence SEQ ID No 7, 2 et 3 ; a) an antibody comprising a light chain variable domain of sequence SEQ ID No 18 and the three heavy chain CDRs of sequence SEQ ID No 7, 2 and 3;
b) un anticorps comprenant un domaine variable de chaîne légère de séquence SEQ ID No 19 et les trois CDR de chaîne lourde de séquence SEQ ID No 7, 2 et 3 ; b) an antibody comprising a light chain variable domain of sequence SEQ ID No. 19 and the three heavy chain CDRs of sequence SEQ ID No. 7, 2 and 3;
c) un anticorps comprenant un domaine variable de chaîne légère de séquence SEQ ID No 20 et les trois CDR de chaîne lourde de séquence SEQ ID No 7, 2 et 3 ; c) an antibody comprising a light chain variable domain of sequence SEQ ID No. 20 and the three heavy chain CDRs of sequence SEQ ID No. 7, 2 and 3;
d) un anticorps comprenant un domaine variable de chaîne légère de séquence SEQ ID No 21 et les trois CDR de chaîne lourde de séquence SEQ ID No 8, 2 et 3 ; et e) un anticorps comprenant un domaine variable de chaîne légère de séquence SEQ ID No 22 et les trois CDR de chaîne lourde de séquence SEQ ID No 7, 2 et 3. d) an antibody comprising a light chain variable domain of sequence SEQ ID No. 21 and the three heavy chain CDRs of sequence SEQ ID No. 8, 2 and 3; and e) an antibody comprising a light chain variable domain of sequence SEQ ID No 22 and the three heavy chain CDRs of sequence SEQ ID No 7, 2 and 3.
Selon un mode de réalisation de l'invention, l'anticorps est un anticorps choisi parmi : According to one embodiment of the invention, the antibody is an antibody chosen from:
a) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 13 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID Noa) an antibody comprising a heavy chain variable domain of sequence SEQ ID No 13 or any sequence having at least 80% identity with SEQ ID No
13 et un domaine variable de chaîne légère de séquence SEQ ID No 18 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 18 ; 13 and a light chain variable domain of sequence SEQ ID No 18 or any sequence having at least 80% identity with SEQ ID No 18;
b) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 14 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID Nob) an antibody comprising a heavy chain variable domain of sequence SEQ ID No 14 or any sequence having at least 80% identity with SEQ ID No
14 et un domaine variable de chaîne légère de séquence SEQ ID No 19 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 19 ; 14 and a light chain variable domain of sequence SEQ ID No 19 or any sequence having at least 80% identity with SEQ ID No 19;
c) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 15 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID Noc) an antibody comprising a heavy chain variable domain of sequence SEQ ID No 15 or any sequence having at least 80% identity with SEQ ID No
15 et un domaine variable de chaîne légère de séquence SEQ ID No 20 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 20 ; And a light chain variable domain of sequence SEQ ID No. 20 or any sequence exhibiting at least 80% identity with SEQ ID No. 20;
d) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 16 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID Nod) an antibody comprising a heavy chain variable domain of sequence SEQ ID No 16 or any sequence having at least 80% identity with SEQ ID No
16 et un domaine variable de chaîne légère de séquence SEQ ID No 21 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 21 ; et e) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 17 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 17 et un domaine variable de chaîne légère de séquence SEQ ID No 22 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 22. 16 and a light chain variable domain of sequence SEQ ID No 21 or any sequence having at least 80% identity with SEQ ID No 21; and e) an antibody comprising a heavy chain variable domain of sequence SEQ ID No 17 or any sequence having at least 80% identity with SEQ ID No 17 and a light chain variable domain of sequence SEQ ID No 22 or any sequence exhibiting at least 80% identity with SEQ ID No 22.
Les anticorps chimériques décrits ici peuvent également être caractérisés par le domaine constant et, plus particulièrement, lesdits anticorps chimériques peuvent être sélectionnés ou conçus tels que, sans limitation, lgG1 , lgG2, lgG3, IgM, IgA, IgD ou IgE. Plus préférentiellement, dans le cadre de la présente invention, lesdits anticorps chimériques sont lgG1 ou lgG4. The chimeric antibodies described herein can also be characterized by the constant domain and, more particularly, said chimeric antibodies can be selected or designed such as, without limitation, IgG1, IgG2, IgG3, IgM, IgA, IgD or IgE. More preferably, in the context of the present invention, said chimeric antibodies are IgG1 or IgG4.
Selon un mode de réalisation de l'invention, l'anticorps est un anticorps chimérique comprenant les domaines variables de chaîne lourde (VH) et de chaîne légère (VL) tels que décrits ci-dessus au format lgG1. Plus préférentiellement, ledit anticorps chimérique comprend un domaine constant pour le VH de séquence SEQ ID No 43 et un domaine Kappa pour le VL de séquence SEQ ID No 45. According to one embodiment of the invention, the antibody is a chimeric antibody comprising the variable domains of heavy chain (VH) and of light chain (VL) as described above in the lgG1 format. More preferably, said chimeric antibody comprises a constant domain for the VH of sequence SEQ ID No 43 and a Kappa domain for the VL of sequence SEQ ID No 45.
Selon un mode de réalisation de l'invention, l'anticorps est un anticorps chimérique comprenant les domaines variables VH et VL tels que décrits ci-dessus au format lgG4. Plus préférentiellement, ledit anticorps chimérique comprend un domaine constant pour le VH de séquence SEQ ID No 44 et un domaine Kappa pour le VL de séquence SEQ ID No 45. According to one embodiment of the invention, the antibody is a chimeric antibody comprising the variable domains VH and VL as described above in the lgG4 format. More preferably, said chimeric antibody comprises a constant domain for the VH of sequence SEQ ID No 44 and a Kappa domain for the VL of sequence SEQ ID No 45.
Dans un autre mode de réalisation préféré mais non limitatif, l'anticorps est choisi parmi : In another preferred but non-limiting embodiment, the antibody is chosen from:
a) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 23 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 23 et une chaîne légère de séquence SEQ ID No 28 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 28 ; a) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 23 or any sequence exhibiting at least 80% identity with SEQ ID No 23 and a light chain of sequence SEQ ID No 28 or any sequence exhibiting at least 80% identity with SEQ ID No 28;
b) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 24 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 24 et une chaîne légère de séquence SEQ ID No 29 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 29 ; b) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 24 or any sequence exhibiting at least 80% identity with SEQ ID No 24 and a light chain of sequence SEQ ID No 29 or any sequence exhibiting at least 80% identity with SEQ ID No 29;
c) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 25 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID v 25 et une chaîne légère de séquence SEQ ID v 30 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 30 ; d) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 26 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 26 et une chaîne légère de séquence SEQ ID No 31 ou toute séquence présentant au moins 80% % d'identité avec SEQ ID No 31 ; et c) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 25 or any sequence exhibiting at least 80% identity with SEQ ID v 25 and a light chain of sequence SEQ ID v 30 or any sequence exhibiting at least 80% identity with SEQ ID No 30; d) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 26 or any sequence exhibiting at least 80% identity with SEQ ID No 26 and a light chain of sequence SEQ ID No 31 or any sequence exhibiting at least 80%% identity with SEQ ID No 31; and
e) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 27 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 27 et une chaîne légère de séquence SEQ ID No 32 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 32. e) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 27 or any sequence exhibiting at least 80% identity with SEQ ID No 27 and a light chain of sequence SEQ ID No 32 or any sequence exhibiting at least 80% identity with SEQ ID No 32.
Pour plus de clarté, le tableau 2 suivant illustre les séquences de VH et VL, respectivement, pour les anticorps chimériques préférés. For clarity, the following Table 2 illustrates the sequences of VH and VL, respectively, for the preferred chimeric antibodies.
Tableau 2 Table 2
Selon un autre aspect spécifique de la présente invention, l'anticorps est un anticorps humanisé caractérisé en ce que les régions constantes de la chaîne légère et de la chaîne lourde dérivées de l'anticorps humain sont respectivement la région lambda ou kappa et les régions gamma-1 , gamma-2 ou gamma-4. According to another specific aspect of the present invention, the antibody is a humanized antibody characterized in that the constant regions of the light chain and of the heavy chain derived from the human antibody are respectively the lambda or kappa region and the gamma regions. -1, gamma-2 or gamma-4.
Dans un mode de réalisation préféré, l'anticorps comprend un domaine variable de chaîne lourde (VH) ayant : In a preferred embodiment, the antibody comprises a heavy chain variable domain (VH) having:
i) les CDR-H1 , CDR-H2 et CDR-H3 des séquences SEQ ID No 7, 2 et 3, respectivement, et i) CDR-H1, CDR-H2 and CDR-H3 of sequences SEQ ID No 7, 2 and 3, respectively, and
ii) les FR1 , FR2 et FR3 dérivés de la lignée germinale humaine IGHV1-46*01 (SEQ ID No 46), et ii) FR1, FR2 and FR3 derived from the human germ line IGHV1-46 * 01 (SEQ ID No 46), and
iii) le FR4 dérivé de la lignée germinale humaine IGHJ4*01 (SEQ ID No 48). iii) FR4 derived from the human germ line IGHJ4 * 01 (SEQ ID No. 48).
Dans un mode de réalisation préféré, l'anticorps comprend un domaine variable de chaîne légère (VL) ayant : In a preferred embodiment, the antibody comprises a light chain variable domain (VL) having:
i) les CDR-L1 , CDR-L2 et CDR-L3 des séquences SEQ ID No 9, 5 et 11 , respectivement, et i) CDR-L1, CDR-L2 and CDR-L3 of the sequences SEQ ID No 9, 5 and 11, respectively, and
ii) les FR1 , FR2 et FR3 dérivés de la lignée germinale humaine IGKV1-39*01 (SEQ ID No 47), et ii) FR1, FR2 and FR3 derived from the human germ line IGKV1-39 * 01 (SEQ ID No 47), and
iii) le FR4 dérivé de la lignée germinale humaine IGKJ4*01 (SEQ ID No 49). iii) FR4 derived from the human germ line IGKJ4 * 01 (SEQ ID No. 49).
Dans un mode de réalisation préféré de l'invention, mais non limitatif, l'anticorps comprend : In a preferred embodiment of the invention, but not limited to, the antibody comprises:
a) une chaîne lourde ayant CDR-H1 , CDR-H2 et CDR-H3 de séquences SEQ ID No 7, 2 et 3, respectivement, et FR1 , FR2 et FR3 dérivées de la lignée germinale humaine IGHV1-46*01 (SEQ ID No 46), et le FR4 dérivé de la lignée germinale humaine IGHJ4*01 (SEQ ID No 48); et a) a heavy chain having CDR-H1, CDR-H2 and CDR-H3 of sequences SEQ ID No 7, 2 and 3, respectively, and FR1, FR2 and FR3 derived from the human germ line IGHV1-46 * 01 (SEQ ID No. 46), and FR4 derived from the human germ line IGHJ4 * 01 (SEQ ID No. 48); and
b) une chaîne légère ayant CDR-L1 , CDR-L2 et CDR-L3 de séquences SEQ ID No 9, 5 et 11 , respectivement, et FR1 , FR2 et FR3 dérivées de la lignée germinale humaine IGKV1-39*01 (SEQ ID No 47) et le FR4 dérivé de la lignée germinale humaine IGKJ4*01 (SEQ ID No 49). b) a light chain having CDR-L1, CDR-L2 and CDR-L3 of sequences SEQ ID No 9, 5 and 11, respectively, and FR1, FR2 and FR3 derived from the human germ line IGKV1-39 * 01 (SEQ ID No. 47) and FR4 derived from the human germ line IGKJ4 * 01 (SEQ ID No. 49).
Dans un mode de réalisation, l'anticorps comprend un domaine variable de chaîne lourde (VH) de séquence SEQ ID No 33 et un domaine variable de chaîne légère (VL) de séquence SEQ ID No 35. Ledit anticorps humanisé sera appelé ci-après hz208F2 (« Variant 1 » ou « Var. 1 »). In one embodiment, the antibody comprises a heavy chain variable domain (VH) of sequence SEQ ID No 33 and a variable chain domain light (VL) of sequence SEQ ID No. 35. Said humanized antibody will be called hereinafter hz208F2 (“Variant 1” or “Var. 1”).
Dans un autre mode de réalisation, l'anticorps comprend un domaine variable de chaîne lourde (VH) de séquence SEQ ID No 33, ladite séquence SEQ ID No 33 comprenant au moins 1 back-mutation choisie parmi les résidus 20, 34, 35, 38, 48, 50, 59, 61 , 62, 70, 72, 74, 76, 77, 79, 82 et 95. In another embodiment, the antibody comprises a heavy chain variable domain (VH) of sequence SEQ ID No 33, said sequence SEQ ID No 33 comprising at least 1 back-mutation chosen from residues 20, 34, 35, 38, 48, 50, 59, 61, 62, 70, 72, 74, 76, 77, 79, 82 and 95.
Dans un autre mode de réalisation, l'anticorps comprend un domaine variable de chaîne lourde (VH) de séquence SEQ ID No 33, ladite séquence SEQ ID No 33 comprenant 2, 3, 4, 5, 6, 7, 8, 9, 10, 1 1 , 12, 13, 14, 15, 16 ou 17 back-mutations choisies parmi les résidus 20, 34, 35, 38, 48, 50, 59, 61 , 62, 70, 72, 74, 76, 77, 79, 82 et 95. In another embodiment, the antibody comprises a heavy chain variable domain (VH) of sequence SEQ ID No 33, said sequence SEQ ID No 33 comprising 2, 3, 4, 5, 6, 7, 8, 9, 10, 1 1, 12, 13, 14, 15, 16 or 17 back mutations chosen from residues 20, 34, 35, 38, 48, 50, 59, 61, 62, 70, 72, 74, 76, 77 , 79, 82 and 95.
Pour plus de clarté, le tableau 3 suivant illustre les back-mutations préférées. For clarity, the following Table 3 illustrates the preferred back mutations.
Tableau 3 Table 3
Dans un mode de réalisation, l'anticorps comprend un domaine variable de chaîne légère (VL) de séquence SEQ ID No 35, ladite séquence SEQ ID No 35 comprenant au moins 1 back-mutation choisie parmi les résidus 22, 53, 55, 65. 71 , 72, 77 et 87. In one embodiment, the antibody comprises a light chain variable domain (VL) of sequence SEQ ID No 35, said sequence SEQ ID No 35 comprising at least 1 back-mutation chosen from residues 22, 53, 55, 65 . 71, 72, 77 and 87.
Dans un mode de réalisation, l'anticorps comprend un domaine variable de chaîne légère (VL) de séquence SEQ ID No 35, ladite séquence de SEQ ID No 35 comprenant 2, 3, 4, 5, 6, 7 ou 8 back-mutations choisies parmi les résidus 22, 53, 55, 65, 71 , 72, 77 ou 87. In one embodiment, the antibody comprises a light chain variable domain (VL) of sequence SEQ ID No 35, said sequence of SEQ ID No 35 comprising 2, 3, 4, 5, 6, 7 or 8 back mutations chosen from residues 22, 53, 55, 65, 71, 72, 77 or 87.
Dans un autre mode de réalisation, l'anticorps comprend : In another embodiment, the antibody comprises:
a) un domaine variable (VH) de chaîne lourde de séquence SEQ ID No 33, dans lequel ladite séquence SEQ ID No 33 comprend au moins 1 back-mutation choisie parmi les résidus 20, 34, 35, 38, 48, 50, 59. 61 , 62, 70, 72, 74, 76, 77, 79, 82 et 95 ; et b) un domaine variable (VL) de chaîne légère de séquence SEQ ID No 35, ladite séquence de SEQ ID No 35 comprenant au moins 1 back-mutation choisie parmi les résidus 22, 53, 55, 65, 71 , 72, 77 et 87. a) a heavy chain variable domain (VH) of sequence SEQ ID No 33, in which said sequence SEQ ID No 33 comprises at least 1 back-mutation chosen from residues 20, 34, 35, 38, 48, 50, 59 61, 62, 70, 72, 74, 76, 77, 79, 82 and 95; and b) a variable domain (VL) of light chain of sequence SEQ ID No 35, said sequence of SEQ ID No 35 comprising at least 1 back-mutation chosen from residues 22, 53, 55, 65, 71, 72, 77 and 87.
Pour plus de clarté, le tableau 4 suivant illustre les back-mutations préférées. For clarity, the following Table 4 illustrates the preferred back mutations.
Tableau 4 Table 4
Dans un tel mode de réalisation, l'anticorps comprend toutes les back- mutations mentionnées ci-dessus et correspond à un anticorps comprenant un domaine variable de chaîne lourde (VH) de séquence SEQ ID No 34 et un domaine variable de chaîne légère (VL) de séquence SEQ ID No 36. Ledit anticorps humanisé sera appelé ci-après hz208F2 (« Variante 3 » ou « Var. 3 »). In such an embodiment, the antibody comprises all the back mutations mentioned above and corresponds to an antibody comprising a heavy chain variable domain (VH) of sequence SEQ ID No 34 and a light chain variable domain (VL ) of sequence SEQ ID No. 36. Said humanized antibody will be called hereinafter hz208F2 (“Variant 3” or “Var. 3”).
Dans un autre mode de réalisation, toutes les formes humanisées comprises entre la variante 1 et la variante 3 sont également englobées par la présente invention. En d'autres termes, l'anticorps correspond à un anticorps comprenant un domaine variable (VH) de chaîne lourde de séquence « consensus » SEQ ID No 41 et un domaine variable de chaîne légère (VL) de séquence « consensus » SEQ ID No 42. L'anticorps humanisé, dans son ensemble, sera appelé ci-après hz208F2 (« Variant 2 » ou « Var. 2 »). In another embodiment, all humanized forms included between Variant 1 and Variant 3 are also encompassed by the present invention. In other words, the antibody corresponds to an antibody comprising a heavy chain variable domain (VH) of “consensus” sequence SEQ ID No. 41 and a light chain variable domain (VL) of “consensus” sequence SEQ ID No. 42. The humanized antibody, as a whole, will be referred to hereinafter as hz208F2 ("Variant 2" or "Var. 2").
Dans un mode de réalisation préféré mais non limitatif, l'anticorps est choisi parmi : In a preferred but non-limiting embodiment, the antibody is chosen from:
a) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 33 ou toute séquence présentant au moins 80%, de préférence 85%, 90%, 95% et 98% d'identité avec la SEQ ID No 33 et les trois chaînes légères CDR de séquences SEQ ID No 9, 5 et 11 ; et a) an antibody comprising a heavy chain variable domain of sequence SEQ ID No 33 or any sequence exhibiting at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No 33 and the three CDR light chains of sequences SEQ ID No 9, 5 and 11; and
b) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 34 ou toute séquence présentant au moins 80%, de préférence 85%, 90%, 95% et 98% d'identité avec la SEQ ID No 34 et les trois chaînes légères CDR de séquences SEQ ID No 9, 5 et 11. Par « toute séquence présentant au moins 80%, de préférence 85%, 90%, 95% et 98% d'identité avec SEQ ID No 33 ou 34 », on entend respectivement les séquences présentant les trois CDR à chaîne lourde SEQ ID No 1 , 2 et 3 et, en outre, présentant au moins 80%, de préférence 85%, 90%, 95% et 98%, d’identité avec la séquence complète SEQ ID No 33 ou 34 en dehors des séquences correspondant aux CDR (c'est-à-dire SEQ ID No 1 , 2 et 3). b) an antibody comprising a heavy chain variable domain of sequence SEQ ID No 34 or any sequence exhibiting at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No 34 and the three CDR light chains of sequences SEQ ID No 9, 5 and 11. By “any sequence exhibiting at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No 33 or 34” is meant respectively the sequences exhibiting the three heavy chain CDRs SEQ ID No 1, 2 and 3 and, in addition, exhibiting at least 80%, preferably 85%, 90%, 95% and 98%, identity with the complete sequence SEQ ID No 33 or 34 apart from the sequences corresponding to the CDRs (i.e. SEQ ID No 1, 2 and 3).
Dans un mode de réalisation de l'invention, l'anticorps est choisi parmi : In one embodiment of the invention, the antibody is chosen from:
a) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 33 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 33 et les trois CDR de chaîne légère des séquences SEQ ID No 9, 5 et 11 ; et b) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 34 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 34 et les trois CDR de chaîne légère des séquences SEQ No NO 9, 5 et 11. a) an antibody comprising a heavy chain variable domain of sequence SEQ ID No 33 or any sequence having at least 80% identity with SEQ ID No 33 and the three light chain CDRs of sequences SEQ ID No 9, 5 and 11; and b) an antibody comprising a heavy chain variable domain of sequence SEQ ID No 34 or any sequence having at least 80% identity with SEQ ID No 34 and the three light chain CDRs of sequences SEQ No NO 9, 5 and 11.
S'il n'est pas indiqué dans les paragraphes concernés, dans la présente description, par une séquence quelconque ou par une séquence présentant au moins 80% d'une séquence particulière, il faut comprendre que ladite séquence présente au moins 80% et de préférence 85%, 90%, 95% et 98% d’identité avec la séquence de référence. Que ces séquences contiennent ou non des séquences de CDR, il est entendu que les séquences présentant au moins ces CDR doivent être identiques aux CDR de la séquence de référence, les identités à 80%, de préférence 85%, 90%, 95% et 98%, avec la séquence complète devant être calculées pour la séquence restante située en dehors des séquences correspondant à ces CDR. If it is not indicated in the paragraphs concerned, in the present description, by any sequence or by a sequence having at least 80% of a particular sequence, it should be understood that said sequence has at least 80% and preferably 85%, 90%, 95% and 98% identity with the reference sequence. Whether or not these sequences contain CDR sequences, it is understood that the sequences exhibiting at least these CDRs must be identical to the CDRs of the reference sequence, the identities at 80%, preferably 85%, 90%, 95% and 98%, with the complete sequence having to be calculated for the remaining sequence lying outside the sequences corresponding to these CDRs.
Dans un mode de réalisation préféré, l'anticorps est choisi parmi : In a preferred embodiment, the antibody is chosen from:
a) un anticorps comprenant un domaine variable de chaîne légère de séquence SEQ ID No 35 ou toute séquence présentant au moins 80%, de préférence 85%, 90%, 95% et 98% d'identité avec la SEQ ID No 35 et les trois chaînes lourdes CDR de séquences SEQ ID No 7, 2 et 3; et a) an antibody comprising a light chain variable domain of sequence SEQ ID No 35 or any sequence exhibiting at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No 35 and the three CDR heavy chains of sequences SEQ ID No 7, 2 and 3; and
b) un anticorps comprenant un domaine variable de chaîne légère de séquence SEQ ID No 36 ou toute séquence présentant au moins 80%, de préférence 85%, 90%, 95% et 98% d'identité avec la SEQ ID No 36 et les trois chaînes lourdes CDR de séquences SEQ ID No 7, 2 et 3. b) an antibody comprising a variable domain of light chain of sequence SEQ ID No 36 or any sequence exhibiting at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No 36 and the three CDR heavy chains of sequences SEQ ID No 7, 2 and 3.
Par « toute séquence présentant au moins 80%, de préférence 85%, 90%, 95% et 98% d'identité avec la SEQ ID No 35 ou 36 », on entend désigner les séquences présentant les trois CDR à chaîne légère SEQ ID No 4, 5 et 6 et, en outre, présentant au moins 80%, de préférence 85%, 90%, 95% et 98%, d’identité avec la séquence complète SEQ ID No 35 ou 36 en dehors des séquences correspondant aux CDR (à savoir SEQ ID No 4, 5 et 6). The expression “any sequence exhibiting at least 80%, preferably 85%, 90%, 95% and 98% identity with SEQ ID No. 35 or 36” is intended to denote the sequences exhibiting the three light chain CDRs SEQ ID No 4, 5 and 6 and, in addition, exhibiting at least 80%, preferably 85%, 90%, 95% and 98%, identity with the complete sequence SEQ ID No 35 or 36 apart from the sequences corresponding to the CDRs (namely SEQ ID No 4, 5 and 6).
Dans un mode de réalisation de l'invention, l'anticorps est choisi parmi : In one embodiment of the invention, the antibody is chosen from:
a) un anticorps comprenant un domaine variable de chaîne légère de séquence SEQ ID No 35 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID Noa) an antibody comprising a light chain variable domain of sequence SEQ ID No 35 or any sequence having at least 80% identity with SEQ ID No
35 et les trois CDR de chaîne lourde de séquences SEQ ID No 7, 2 et 3; et b) un anticorps comprenant un domaine variable de chaîne lourde de séquence SEQ ID No 36 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID NoAnd the three heavy chain CDRs of sequences SEQ ID Nos. 7, 2 and 3; and b) an antibody comprising a heavy chain variable domain of sequence SEQ ID No 36 or any sequence having at least 80% identity with SEQ ID No
36 et les trois CDR de chaîne lourde de séquences SEQ ID No 7, 2 et 3. 36 and the three heavy chain CDRs of sequences SEQ ID No 7, 2 and 3.
Les anticorps humanisés décrits ici peuvent également être caractérisés par le domaine constant et, plus particulièrement, lesdits anticorps humanisés peuvent être sélectionnés notamment parmi lgG1 , lgG2, lgG3, IgM, IgA, IgD ou IgE. Plus préférablement, dans le contexte de la présente invention, lesdits anticorps humanisés sont lgG1 ou lgG4. The humanized antibodies described here can also be characterized by the constant domain and, more particularly, said humanized antibodies can be selected in particular from lgG1, lgG2, lgG3, IgM, IgA, IgD or IgE. More preferably, in the context of the present invention, said humanized antibodies are IgG1 or IgG4.
Selon un mode de réalisation de l'invention, l'anticorps est un anticorps humanisé comprenant les domaines variables VH et VL tels que décrits ci-dessus au format lgG1. Plus préférentiellement, ledit anticorps humanisé comprend un domaine constant pour le VH de séquence SEQ ID No 43 et un domaine Kappa pour le VL de séquence SEQ ID No 45. According to one embodiment of the invention, the antibody is a humanized antibody comprising the variable domains VH and VL as described above in the lgG1 format. More preferably, said humanized antibody comprises a constant domain for the VH of sequence SEQ ID No 43 and a Kappa domain for the VL of sequence SEQ ID No 45.
Selon un mode de réalisation de l'invention, l'anticorps est un anticorps humanisé comprenant les domaines variables VH et VL tels que décrits ci-dessus au format lgG4. Plus préférentiellement, ledit anticorps humanisé comprend un domaine constant pour le VH de séquence SEQ ID No 44 et un domaine Kappa pour le VL de séquence SEQ ID No 45. According to one embodiment of the invention, the antibody is a humanized antibody comprising the variable domains VH and VL as described above in the lgG4 format. More preferably, said humanized antibody comprises a constant domain for the VH of sequence SEQ ID No 44 and a Kappa domain for the VL of sequence SEQ ID No 45.
Selon encore un autre mode de réalisation de l'invention, l'anticorps est choisi parmi : According to yet another embodiment of the invention, the antibody is chosen from:
a) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 37 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 37 et une chaîne légère de séquence SEQ ID No 39 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 39 ; et b) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 38 ou toute séquence présentant au moins 80% d'identité avec la SEQ No 38 et une chaîne légère de séquence SEQ ID No 40 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 40. a) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 37 or any sequence exhibiting at least 80% identity with SEQ ID No 37 and a light chain of sequence SEQ ID No 39 or any sequence exhibiting at least 80% identity with SEQ ID No 39; and b) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 38 or any sequence exhibiting at least 80% identity with SEQ No 38 and a light chain of sequence SEQ ID No 40 or any sequence exhibiting at least 80 % identity with SEQ ID No 40.
Pour plus de clarté, le tableau 5a suivant illustre des exemples non limitatifs de séquences de VH et VL pour le variant 1 (Var. 1) et le variant 3 (Var. 3) de l'anticorps humanisé hz208F2. Il comprend également la séquence consensus pour le variant 2 (Var. 2). For greater clarity, the following Table 5a illustrates non-limiting examples of VH and VL sequences for variant 1 (Var. 1) and variant 3 (Var. 3) of the humanized antibody hz208F2. It also includes the consensus sequence for variant 2 (Var. 2).
Tableau 5a Table 5a
Dans un autre mode de réalisation préféré, l'anticorps est choisi parmi : In another preferred embodiment, the antibody is chosen from:
a) un anticorps comprenant un domaine variable de séquence de chaîne lourde choisi parmi les SEQ ID No 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 et 54 ou toute séquence d'au moins 80%, de préférence d’au moins 85%, 90%, 95% et 98% d’identité avec SEQ ID No 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 et 54; et les trois CDR de chaînes légères de séquences SEQ ID No 9, 5 et 11 ; a) an antibody comprising a variable domain of heavy chain sequence chosen from SEQ ID Nos 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 and 54 or any sequence of at least 80%, preferably at least 85%, 90%, 95% and 98% identity with SEQ ID No 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 and 54; and the three CDRs of light chains of sequences SEQ ID No 9, 5 and 11;
b) un anticorps comprenant un domaine variable de séquence de chaîne légère choisi parmi les SEQ ID No 57 ou 60 ou toute séquence présentant au moins 80%, de préférence au moins 85%, 90%, 95% et 98% d'identité avec SEQ ID No 57 ou 60; et les trois CDR de chaînes lourdes de séquences SEQ ID No 7, 2 et 3; et b) an antibody comprising a variable domain of light chain sequence chosen from SEQ ID No 57 or 60 or any sequence exhibiting at least 80%, preferably at least 85%, 90%, 95% and 98% identity with SEQ ID No 57 or 60; and the three CDRs of heavy chains of sequences SEQ ID No 7, 2 and 3; and
c) un anticorps comprenant un domaine variable de séquence de chaîne lourde choisi parmi les SEQ ID No 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 et 54 ou toute séquence d'au moins 80%, de préférence d'au moins 85 %, 90%, 95% et 98% d'identité avec les SEQ ID No 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 et 54; et un domaine variable de chaîne légère choisi parmi SEQ ID No 57 ou 60 ou toute séquence ayant au moins 80%, de préférence au moins 85%, 90%, 95% et 98% d’identité avec SEQ ID No 57 ou 60. c) an antibody comprising a variable domain of heavy chain sequence chosen from SEQ ID Nos 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 and 54 or any sequence at least 80%, preferably at least 85%, 90%, 95% and 98% identity with SEQ ID Nos 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 and 54; and a light chain variable domain chosen from SEQ ID No 57 or 60 or any sequence having at least 80%, preferably at least 85%, 90%, 95% and 98% identity with SEQ ID No 57 or 60.
Selon encore un autre mode de réalisation de l'invention, l'anticorps est choisi parmi: According to yet another embodiment of the invention, the antibody is chosen from:
a) un anticorps comprenant une chaîne lourde de séquence SEQ ID No 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 et 54 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 ou 54, et une chaîne légère de séquence SEQ ID No 57 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 57 ; et a) an antibody comprising a heavy chain of sequence SEQ ID No 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 and 54 or any sequence having at least 80% identity with SEQ ID No 56, 62, 64, 66, 68, 70, 72, 74, 76, 78 or 54, and a light chain of sequence SEQ ID No. 57 or any sequence having at least 80% identity with SEQ ID No. 57; and
b) un anticorps comprenant une chaîne lourde de séquence SEQ ID No 56, 64, 68 et 78 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 56, 64, 68 ou 78 et une chaîne légère de séquence SEQ ID No 60, ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 60. b) an antibody comprising a heavy chain of sequence SEQ ID No 56, 64, 68 and 78 or any sequence having at least 80% identity with SEQ ID No 56, 64, 68 or 78 and a light chain of sequence SEQ ID No. 60, or any sequence exhibiting at least 80% identity with SEQ ID No. 60.
Selon encore un autre mode de réalisation de l'invention, l'anticorps est choisi parmi : According to yet another embodiment of the invention, the antibody is chosen from:
a) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 58 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 58 et une chaîne légère de séquence SEQ ID No 59 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 59 ; a) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 58 or any sequence exhibiting at least 80% identity with SEQ ID No 58 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59;
b) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 58 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 58 et une chaîne légère de séquence SEQ ID No 61 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 61 ; b) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 58 or any sequence exhibiting at least 80% identity with SEQ ID No 58 and a light chain of sequence SEQ ID No 61 or any sequence exhibiting at least 80% identity with SEQ ID No 61;
c) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 63 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 63 et une chaîne légère de séquence SEQ ID No 59 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 59 ; d) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 65 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 65 et une chaîne légère de séquence SEQ ID No 59 ou toute séquence présentant au moins 80% % d'identité avec SEQ ID No 59 ; c) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 63 or any sequence exhibiting at least 80% identity with SEQ ID No 63 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59; d) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 65 or any sequence exhibiting at least 80% identity with SEQ ID No 65 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80%% identity with SEQ ID No 59;
e) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 65 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 65 et une chaîne légère de séquence SEQ ID No 61 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 61 ; e) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 65 or any sequence exhibiting at least 80% identity with SEQ ID No 65 and a light chain of sequence SEQ ID No 61 or any sequence exhibiting at least 80% identity with SEQ ID No 61;
f) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 67 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 67 et une chaîne légère de séquence SEQ ID No 59 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 59 ; f) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 67 or any sequence exhibiting at least 80% identity with SEQ ID No 67 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59;
g) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 69 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 69 et une chaîne légère de séquence SEQ ID No 59 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 59 ; g) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 69 or any sequence exhibiting at least 80% identity with SEQ ID No 69 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59;
h) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 69 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 69 et une chaîne légère de séquence SEQ ID No 61 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 61 ; h) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 69 or any sequence exhibiting at least 80% identity with SEQ ID No 69 and a light chain of sequence SEQ ID No 61 or any sequence exhibiting at least 80% identity with SEQ ID No 61;
i) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 71 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 71 et une chaîne légère de séquence SEQ ID No 59 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 59 ; i) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 71 or any sequence exhibiting at least 80% identity with SEQ ID No 71 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59;
j) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 73 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 73 et une chaîne légère de séquence SEQ ID No 59 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 59 ; j) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 73 or any sequence exhibiting at least 80% identity with SEQ ID No 73 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59;
k) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 75 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 75 et une chaîne légère de séquence SEQ ID No 59 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 59 ; I) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 77 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 77 et une chaîne légère de séquence SEQ ID No 59 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 59 ; k) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 75 or any sequence exhibiting at least 80% identity with SEQ ID No 75 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59; I) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 77 or any sequence exhibiting at least 80% identity with SEQ ID No 77 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59;
m) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 53 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 53 et une chaîne légère de séquence SEQ ID No 59 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 59 ; m) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 53 or any sequence exhibiting at least 80% identity with SEQ ID No 53 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59;
n) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 53 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 53 et une chaîne légère de séquence SEQ ID No 61 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 61 ; et n) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 53 or any sequence exhibiting at least 80% identity with SEQ ID No 53 and a light chain of sequence SEQ ID No 61 or any sequence exhibiting at least 80% identity with SEQ ID No 61; and
o) un anticorps comprenant ou consistant en une chaîne lourde de séquence SEQ ID No 55 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 55 et une chaîne légère de séquence SEQ ID No 59 ou toute séquence présentant au moins 80% d'identité avec SEQ ID No 59. o) an antibody comprising or consisting of a heavy chain of sequence SEQ ID No 55 or any sequence exhibiting at least 80% identity with SEQ ID No 55 and a light chain of sequence SEQ ID No 59 or any sequence exhibiting at least 80% identity with SEQ ID No 59.
En d'autres termes, l'anticorps peut être un anticorps comprenant : In other words, the antibody can be an antibody comprising:
a) une chaîne lourde de séquence sélectionnée parmi les SEQ ID No 58, 63, 65, 67, 69, 71 , 73, 75, 77, 53 et 55 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 58, 63, 65, 67, 69, 71 , 73, 75, 77, 53 et 55 ; et a) a heavy chain of sequence selected from SEQ ID No 58, 63, 65, 67, 69, 71, 73, 75, 77, 53 and 55 or any sequence having at least 80% identity with SEQ ID No 58, 63, 65, 67, 69, 71, 73, 75, 77, 53 and 55; and
b) une chaîne légère de séquence sélectionnée parmi les SEQ ID No 59 et 61 ou toute séquence présentant au moins 80% d'identité avec les SEQ ID No 59 et 61. b) a light chain of sequence selected from SEQ ID Nos 59 and 61 or any sequence exhibiting at least 80% identity with SEQ ID Nos 59 and 61.
Dans un mode de réalisation de l'invention, l'anticorps est choisi parmi : In one embodiment of the invention, the antibody is chosen from:
a) une chaîne lourde de séquence sélectionnée parmi les SEQ ID No 58, 63, 65, 67, 69, 71 , 73, 75, 77, 53 et 55 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 58, 63, 65, 67, 69, 71 , 73, 75, 77, 53 ou 55; et a) a heavy chain of sequence selected from SEQ ID No 58, 63, 65, 67, 69, 71, 73, 75, 77, 53 and 55 or any sequence having at least 80% identity with SEQ ID No 58, 63, 65, 67, 69, 71, 73, 75, 77, 53 or 55; and
b) une chaîne légère de séquence sélectionnée parmi les SEQ ID No 59 et 61 ou toute séquence présentant au moins 80% d'identité avec la SEQ ID No 59 ou 61. b) a light chain of sequence selected from SEQ ID No 59 and 61 or any sequence exhibiting at least 80% identity with SEQ ID No 59 or 61.
Pour plus de clarté, le tableau 5b suivant illustre des exemples non limitatifs de séquences de VH et VL (domaine variable et longueur complète) pour différents variants de l'anticorps humanisé hz208F2. Table 5b For greater clarity, the following Table 5b illustrates non-limiting examples of VH and VL sequences (variable domain and full length) for different variants of the humanized antibody hz208F2. Table 5b
Selon un autre aspect de la présente invention, l'anticorps est un anticorps produit par l'hybridome 1-4757, 1-4773, 1-4775, 1-4736 ou 1-4774 déposé à la CNCM de l'Institut Pasteur France les 30 mai 2013, 26 juin 2013, 26 juin 2013, 24 avril 2013 et 26 juin 2013, respectivement. L’anticorps est plus particulièrement un anticorps 208F2 (par ex. chimérique ou humanisé, notamment chimérique) et plus particulière un anticorps c208F2 qui est un anticorps monoclonal (lgG1). Cet anticorps est notamment décrit dans WO2015162291 et est caractérisé en ce qu’il comprend les trois CDR de chaîne légère de séquence SEQ ID Nos. 9, 5 et11 respectivement, et les trois CDR de chaîne lourde de séquence SEQ ID Nos 7, 2 et 3 respectivement. L’anticorps est en outre caractérisé en ce qu’il comprend un domaine variable de la chaîne légère de séquence SEQ ID No 18 et un domaine variable de chaîne lourde de séquence SEQ ID No 13. L’anticorps est enfin caractérisé en ce qu’il comprend une chaîne légère de séquence SEQ ID No 28 et un domaine variable de chaîne lourde de séquence SEQ ID No 23. According to another aspect of the present invention, the antibody is an antibody produced by the hybridoma 1-4757, 1-4773, 1-4775, 1-4736 or 1-4774 deposited at the CNCM of the Institut Pasteur France. May 30, 2013, June 26, 2013, June 26, 2013, April 24, 2013 and June 26, 2013, respectively. The antibody is more particularly a 208F2 antibody (eg chimeric or humanized, in particular chimeric) and more particularly a c208F2 antibody which is a monoclonal antibody (IgG1). This antibody is in particular described in WO2015162291 and is characterized in that it comprises the three light chain CDRs of sequence SEQ ID Nos. 9, 5 and 11 respectively, and the three heavy chain CDRs of sequence SEQ ID Nos. 7, 2 and 3 respectively. The antibody is further characterized in that it comprises a variable domain of the light chain of sequence SEQ ID No 18 and a variable domain of heavy chain of sequence SEQ ID No 13. The antibody is finally characterized in that it comprises a light chain of sequence SEQ ID No 28 and a heavy chain variable domain of sequence SEQ ID No 23.
L’anticorps c208F2 et l’ADC-A peuvent être obtenus par toutes les méthodes connues de l’homme du métier d’obtention d’anticorps et d’ADC. Ils sont notamment obtenus par les méthodes décrites dans la demande WO2015162291 (ADC-A correspond de préférence à l’ADC nommé C208F2-G-13 dans WO2015162291). The c208F2 antibody and ADC-A can be obtained by any of the methods known to those skilled in the art of obtaining antibodies and ADC. They are obtained in particular by the methods described in application WO2015162291 (ADC-A preferably corresponds to the ADC named C208F2-G-13 in WO2015162291).
Traitement Treatment
Par « résistance » selon l’invention, on entend que le patient ne présente plus de réponse au traitement, c’est-à-dire qu’il y a reprise de la progression du cancer ou stagnation. By "resistance" according to the invention is meant that the patient no longer shows a response to treatment, that is to say that there is resumption of cancer progression or stagnation.
Par « traitement » selon l’invention, on entend notamment une augmentation de la survie globale, et/ou une augmentation de la durée de survie sans progression et/ou une augmentation de la survie sans aggravation et/ou une diminution de la récurrence et/ou une diminution de la taille de la tumeur. By “treatment” according to the invention is meant in particular an increase in overall survival, and / or an increase in the duration of progression-free survival and / or an increase in survival without worsening and / or a decrease in recurrence and / or a decrease in the size of the tumor.
L’évaluation de ces critères de réponse tumorale (résistance et traitement) est bien connue de l’homme du métier et pourra notamment être mesurée par les critères RECIST (Eisenhauer et al Eur J Cancer, 45 (2009) : 228-247 ou ses mises à jour). The evaluation of these tumor response criteria (resistance and treatment) is well known to those skilled in the art and may in particular be measured by the RECIST criteria (Eisenhauer et al Eur J Cancer, 45 (2009): 228-247 or its updates).
La maladie proliférative sera plus particulièrement un cancer, et notamment un cancer résistant au docétaxel. The proliferative disease will be more particularly a cancer, and in particular a cancer resistant to docetaxel.
Le cancer selon l’invention pourra notamment être sélectionné parmi le cancer du sein, du colon, mélanome, du poumon dont du poumon non à petites cellules, gastrique, des voies aéro-digestives supérieures, de l’œsophage, colorectal, gastrique, gliome, de l’œsophage, de l’ovaire, de la prostate, rénal, de la thyroïde, de l’utérus, oral squameux, mésothéliome. The cancer according to the invention may in particular be selected from cancer of the breast, colon, melanoma, lung including non-small cell lung, gastric, upper aero-digestive tract, esophagus, colorectal, gastric, glioma, esophagus, ovary, prostate, renal, thyroid, uterus, oral squamous, mesothelioma.
Dans un mode de réalisation particulier, le cancer traité selon l’invention sera un cancer habituellement traité par le docétaxel notamment les cancers gastriques, de la prostate, du poumon (dont cancer du poumon non à petites cellules), du sein et des voies aéro-digestives supérieures. In a particular embodiment, the cancer treated according to the invention will be a cancer usually treated with docetaxel, in particular gastric, prostate, lung (including non-small cell lung cancer), breast and airway cancers. -digestive superior.
Dans un mode de réalisation particulier, le cancer traité selon l’invention sera un cancer comprenant des cellules tumorales exprimant ou sur-exprimant tout ou partie de la protéine IGF-1 R. Les cancers exprimant IGF-1 R pourront être des cancers exprimant initialement IGF-1 R ou des cancers qui n’exprimait pas initialement IGF-1 R mais qui se sont mis à l’exprimer après être devenu résistant à un premier traitement (ou plus), tel que résistant au docétaxel. In a particular embodiment, the cancer treated according to the invention will be a cancer comprising tumor cells expressing or overexpressing all or part of the IGF-1 R protein. Cancers expressing IGF-1 R may be cancers initially expressing IGF-1 R or cancers which did not initially express IGF-1 R but which started expressing it after becoming resistant to a first treatment (or more), such as resistant to docetaxel.
Dans un mode de réalisation, l’ADC-A pourra être administré après apparition d’une résistance au docétaxel. ADC-A pourra alors être administré seul, postérieurement au docétaxel ou de façon concomitante avec le docétaxel et/ou une autre chimiothérapie. L’initiation du traitement par ADC-A pourra notamment débuter immédiatement après la constatation de la survenue de la résistance, ou dans les 1 , 2, 3, 4, 5, 6, 7, ou encore 8 semaines ou plus après la constatation de la survenue de la résistance, notamment avant 16 semaines suivant la constatation de la survenue de la résistance. In one embodiment, ADC-A could be administered after the development of resistance to docetaxel. ADC-A can then be administered alone, after docetaxel or concomitantly with docetaxel and / or other chemotherapy. In particular, the initiation of treatment with ADC-A may begin immediately after the observation of resistance, or within 1, 2, 3, 4, 5, 6, 7, or even 8 weeks or more after the observation of resistance. the occurrence of resistance, particularly before 16 weeks following the observation of the occurrence of resistance.
Dans un autre mode de réalisation, l’ADC-A pourra être administré avant l’apparition de la résistance au docétaxel, de manière concomitante au docétaxel. L’initiation du traitement par ADC-A pourra alors être initié en même temps ou après le traitement au docétaxel mais avant l’apparition d’une résistance au docétaxel.. In another embodiment, ADC-A could be administered prior to the onset of resistance to docetaxel, concomitantly with docetaxel. The initiation of treatment with ADC-A can then be initiated at the same time as or after treatment with docetaxel but before the development of resistance to docetaxel.
Par « de manière concomitante » on entend que les produits sont administrés de manière à être présent en même temps dans l’organisme du patient. Les produits peuvent être administrés en même temps ou de manière séquentielle. By "concomitantly" is meant that the products are administered so as to be present at the same time in the body of the patient. The products can be administered simultaneously or sequentially.
Par « de manière postérieure » ou « postérieurement » on entend que l’initiation du traitement par le premier produit suit le traitement par le second produit, par exemple que le traitement par ADC-A suit le traitement par le docétaxel. Les deux produits ne sont donc pas simultanément présents dans l’organisme du patient. By "posteriorly" or "subsequently" is meant that the initiation of treatment with the first product follows treatment with the second product, for example that treatment with ADC-A follows treatment with docetaxel. The two products are therefore not simultaneously present in the patient's body.
La posologie du docétaxel dépendra de la gravité, de l’état du patient et du type de cancer à traiter. Elle pourra aussi varier en fonction des traitements préalablement ou concomitamment reçus par le patient. De manière générale, le docétaxel sera administré à une dose comprise entre 50mg/m2 de surface corporelle (BSA - Body surface area) et 125 mg/m2 notamment entre 75 mg/m2 et 100 mg/m2 toute les 1 à 4 semaines notamment toutes les trois semaines. The dosage of docetaxel will depend on the severity and condition of the patient and the type of cancer to be treated. It may also vary depending on the treatments previously or concomitantly received by the patient. Generally, docetaxel is administered at a dose between 50mg / m 2 body surface area (BSA - Body area surface) and 125 mg / m 2, in particular between 75 mg / m 2 and 100 mg / m 2 every 1 to 4 weeks in particular every three weeks.
Le nombre de cycles de traitement (c’est-à-dire le nombre d’occurrences de l’administration du traitement et du temps entre deux administrations) dépendra de la réponse du patient et de l’apparition d’une résistance au docétaxel. Il pourra notamment être compris entre 3 et 12 cycles ou plus. The number of treatment cycles (that is, the number of times the treatment is administered and the time between two doses) will depend on the patient's response and the development of resistance to docetaxel. It may in particular be between 3 and 12 cycles or more.
La posologie de l’ADC-A dépendra de la gravité, de l’état du patient et du type de cancer à traité. Elle pourra aussi varier en fonction des traitements antérieurement ou concomitamment reçus par le patient. De manière générale, ADC-A sera administré à une dose comprise entre 0,5 et 3 mg/kg de patient à traiter, notamment entre 0,9 et 2,5 mg/kg de patient à traiter, toutes les 1 à 4 semaines notamment toutes les trois semaines. The dosage of ADC-A will depend on the severity and condition of the patient and the type of cancer being treated. It may also vary depending on the treatments previously or concomitantly received by the patient. In general, ADC-A will be administered at a dose of between 0.5 and 3 mg / kg of patient to be treated, in particular between 0.9 and 2.5 mg / kg of patient to be treated, every 1 to 4 weeks especially every three weeks.
Le nombre de cycles de traitement par ADC-A dépendra notamment de la réponse du patient. Il pourra notamment être compris entre 1 et 18 cycles ou plus jusqu’à reprise de la progression de la tumeur ou jusqu’à la rémission The number of cycles of treatment with ADC-A will depend in particular on the patient's response. It may in particular be between 1 and 18 cycles or more until the progression of the tumor resumes or until remission
Le traitement selon l’invention pourra être combiné avec d’autres traitements anti-cancéreux préalablement et/ou concomitamment au docétaxel et/ ou à l’ADC-A. Notamment le traitement anti-cancéreux est un traitement avec une molécule choisie dans le groupe constitué par la doxorubicine, le cyclophosphamide, la capécitabine, le cisplatine, le paclitaxel, la carboplatine, le lapatinib, le pertuzimab, le bevacizumab, le trastuzumab, le 5-fluorouracile, l’anthracycline, la vinorelbine, le binimetinib, l’encorafenib et le neratinib. Le traitement selon l’invention pourra aussi être combiné avec d’autres types de médicaments tels que les corticoïdes, notamment la dexaméthasone ou la prednisone. The treatment according to the invention may be combined with other anti-cancer treatments before and / or concomitantly with docetaxel and / or ADC-A. In particular, the anti-cancer treatment is a treatment with a molecule chosen from the group consisting of doxorubicin, cyclophosphamide, capecitabine, cisplatin, paclitaxel, carboplatin, lapatinib, pertuzimab, bevacizumab, trastuzumab, 5 -fluorouracil, anthracycline, vinorelbine, binimetinib, encorafenib and neratinib. The treatment according to the invention may also be combined with other types of drugs such as corticosteroids, in particular dexamethasone or prednisone.
La présente invention porte en outre sur une composition pharmaceutique comprenant ADC-A et au moins un excipient pharmaceutiquement acceptable pour son utilisation selon l’invention. Notamment ADC-A sera formulé de manière à pouvoir être injecté par voie intraveineuse. EXEMPLE : The present invention further relates to a pharmaceutical composition comprising ADC-A and at least one pharmaceutically acceptable excipient for its use according to the invention. In particular ADC-A will be formulated so that it can be injected intravenously. EXAMPLE:
Matériel et méthode Material and method
Cellules : les cellules MCF-7 sont obtenues de l'ATTC (Manassas). Les cellules sont maintenues dans un incubateur à 5 % de C02, 90 % d'humidité et 37°C dans un milieu de culture cellulaire standard, tel que recommandé par le fournisseur. Cells: MCF-7 cells are obtained from ATTC (Manassas). The cells are maintained in an incubator at 5% CO2, 90% humidity and 37 ° C in standard cell culture medium, as recommended by the supplier.
Génération de l'anticorps : L’anticorps 208F2 est produit comme décrit dans la demande WO2015162291. Succinctement, l’anticorps anti-IGF-1 R, c208F2 humanisé (hz208F2(4)) est généré en utilisant la technologie des hybridomes. Des souris Balb/c sont immunisées avec la protéine humaine recombinante IGF-1 R (rhlGF-1 R) (systèmes R&D) en présence d'adjuvant de Freund. Les rates sont fusionnées avec le partenaire de fusion du myélome SP2/0. Après le clonage par dilution limite, la liaison et l'internalisation de l’anticorps aux cellules MCF-7 est confirmée et l'isotype déterminé. La spécificité de liaison est vérifiée par ELISA sur du rhlGF-1 R, du récepteur recombinant de l'insuline humaine (rhIR) et de l'IGF-1 R murin (mlGF-1 R) (systèmes R&D). L'anticorps m208F2 est ensuite humanisé par greffe des régions déterminant la complémentarité (CDR) et exprimé dans des cellules ovariennes de hamster chinois pour une caractérisation pharmacologique complète. Generation of the antibody: The 208F2 antibody is produced as described in application WO2015162291. Briefly, the anti-IGF-1 R antibody, humanized c208F2 (hz208F2 (4)) is generated using hybridoma technology. Balb / c mice are immunized with the recombinant human protein IGF-1 R (rhlGF-1 R) (R&D systems) in the presence of Freund's adjuvant. The spleens are fused with the myeloma fusion partner SP2 / 0. After limiting dilution cloning, binding and internalization of the antibody to MCF-7 cells is confirmed and the isotype determined. The binding specificity is verified by ELISA on rhlGF-1 R, the recombinant human insulin receptor (rhIR) and murine IGF-1 R (mlGF-1 R) (R&D systems). The m208F2 antibody is then humanized by complementarity determining regions (CDRs) grafting and expressed in Chinese hamster ovary cells for complete pharmacological characterization.
Production et caractérisation de ADC-A : ADC-A est produit comme décrit dans la demande WO2015162291 (ADC-A correspond à l’ADC nommé C208F2-G-13 de WO2015162291). Une légère réduction du mAb 208F2 (hz208F2-4) et le couplage au linker payload est effectué comme décrit précédemment (Sun et al. Bioconjug. Chem 2005 ; 16 : 1282-90, Wagner-Rousset et al Mabs 2014 ; 6 : 173-84). Brièvement, pour cibler un DAR de 4, le hz208F2-4 a été réduit avec 2,5 équivalents molaires de tris(2- carboxyéthyl)phosphine (TCEP). L'anticorps réduit a ensuite été traité avec 7 équivalents molaires de linker-payload (G-13). Après conjugaison, ADC-A est concentré à 5 mg/mL (dans du tampon dans 25 mM d'histidine pH 6,5,150 mM NaCI et 6% de saccharose). Du Tween 80 a ensuite été ajouté pour obtenir une concentration finale de 0,005% (v/v). Le produit est finalement filtré à travers un filtre Stericup (GP Express PLUS Membrane, 0.22pm, Polyethersulfone, Millipore) et conservé à 4°C. Production and characterization of ADC-A: ADC-A is produced as described in application WO2015162291 (ADC-A corresponds to the ADC named C208F2-G-13 of WO2015162291). A slight reduction of mAb 208F2 (hz208F2-4) and coupling to the payload linker is carried out as described previously (Sun et al. Bioconjug. Chem 2005; 16: 1282-90, Wagner-Rousset et al Mabs 2014; 6: 173- 84). Briefly, to target a DAR of 4, hz208F2-4 was reduced with 2.5 molar equivalents of tris (2-carboxyethyl) phosphine (TCEP). The reduced antibody was then treated with 7 molar equivalents of linker-payload (G-13). After conjugation, ADC-A is concentrated to 5 mg / mL (in buffer in 25 mM histidine pH 6.5, 150 mM NaCl and 6% sucrose). Tween 80 was then added to obtain a final concentration of 0.005% (v / v). The product is finally filtered through a Stericup filter (GP Express PLUS Membrane, 0.22pm, Polyethersulfone, Millipore) and stored at 4 ° C.
Détermination de l'activité in vivo : L’activité in vivo est testée dans un modèle de cancer du sein : des souris nudes femelles de 7 semaines (Charles River Laboratories, n=15) ont été greffées par voie sous-cutanée avec 5 c 106 cellules MCF- 7 et ce 1 jour après implantation sous-cutanée de 0,72 mg de granules libérant pendant 60 jours du "^-estradiol (Innovative Research of America). Determination of the in vivo activity: The in vivo activity is tested in a breast cancer model: 7 week old female nude mice (Charles River Laboratories, n = 15) were grafted subcutaneously with 5 c 10 6 MCF- cells 7 and this 1 day after subcutaneous implantation of 0.72 mg of granules releasing for 60 days β -estradiol (Innovative Research of America).
Les souris sont randomisées, et le traitement est amorcé lorsque les tumeurs atteignent une taille d'environ 150 mm3. Le volume tumoral (longueur c largeur c hauteur c 0,52) est mesuré au moins deux fois par semaine et la réponse thérapeutique est définie à l'aide des critères d'évaluation de la réponse des tumeurs solides (RECIST). The mice are randomized, and treatment is initiated when the tumors reach a size of approximately 150 mm 3 . The tumor volume (length c width c height c 0.52) is measured at least twice a week and the therapeutic response is defined using the criteria for evaluating the response of solid tumors (RECIST).
Les souris porteuses de tumeurs MCF-7 sont injectées par voie intraveineuse avec du docétaxel, 9 mg/kg deux fois par semaine, avec un total de 5 injections. Lorsque les tumeurs sont devenues résistantes au docétaxel, les souris sont divisées en 2 groupes de 5 animaux : le groupe 1 reçoit 9 mg/kg de docétaxel toutes les 2 semaines et le groupe 2 reçoit une injection unique de ADC-A de 3 mg/kg. Mice bearing MCF-7 tumors are injected intravenously with docetaxel, 9 mg / kg twice weekly, with a total of 5 injections. When the tumors have become resistant to docetaxel, the mice are divided into 2 groups of 5 animals: group 1 receives 9 mg / kg of docetaxel every 2 weeks and group 2 receives a single injection of ADC-A of 3 mg / kg.
Le pourcentage des valeurs de régression est calculé à l'aide de la formule suivante : The percentage of regression values is calculated using the following formula:
Régression % = 100 cDT/Tinitial Regression% = 100 c DT / Tinitial
où T = le volume de la tumeur dans le groupe traité, DT = le volume de la tumeur dans le groupe traité le jour de l'étude moins le volume de la tumeur dans le groupe traité au jour initial de l'administration, et Tinitial = le volume de la tumeur dans le groupe traité au jour initial de l'administration. La maladie est considérée comme évolutive lorsque la taille de la tumeur augmente de > 20 %. La régression partielle where T = the volume of the tumor in the treated group, DT = the volume of the tumor in the treated group on the day of the study minus the volume of the tumor in the treated group on the initial day of administration, and Tinitial = the volume of the tumor in the treated group on the initial day of administration. The disease is considered progressive when the size of the tumor increases by> 20%. Partial regression
(RP) est définie comme une diminution de la taille de la tumeur > 30 %. L'absence de croissance tumorale, ou une légère diminution (< 30 %), ou une légère augmentation (< 20 %) de la taille de la tumeur est définie comme une maladie stable (ET), et une absence de masse tumorale palpable est définie comme une régression complète (RC). (PR) is defined as a decrease in tumor size> 30%. Lack of tumor growth, or a slight decrease (<30%), or slight increase (<20%) in tumor size is defined as stable disease (SD), and an absence of palpable tumor mass is defined as a complete regression (CR).
Résultats Results
Afin d’évaluer le potentiel thérapeutique de ADC-A dans le cancer du sein, l’effet de l’administration d’ADC-A a été étudié dans un modèle de souris greffées par des cellules MCF-7 après apparition d’une résistance au docétaxel. Après 70 jours, les tumeurs sont devenues résistantes au docétaxel et ont rechuté (Fig. 1). L'administration d'une dose unique d’ADC-A de 3 mg/kg chez des souris atteintes de tumeurs résistantes au docétaxel induit une inhibition forte et significative de la croissance tumorale (P 0,05) (Fig. 1), On observe une RC chez 1 souris et une RP chez 3 souris sur 5. ADC-A et le docétaxel présente un effet synergique. On peut en conclure que ADC-A est un bon traitement seul ou en combinaison avec le docétaxel pour le traitement des tumeurs résistantes au docétaxel. Ceci est d’autant plus surprenant que le payload utilisé à un mécanisme d’action proche (action sur la tubuline) des taxanes et donc du docétaxel. In order to assess the therapeutic potential of ADC-A in breast cancer, the effect of ADC-A administration was studied in a mouse model grafted with MCF-7 cells after the appearance of resistance. with docetaxel. After 70 days, the tumors became resistant to docetaxel and relapsed (Fig. 1). Administration of a single dose of ADC-A of 3 mg / kg in mice with tumors resistant to docetaxel induces a strong and significant inhibition of tumor growth (P 0.05) (Fig. 1), CR is observed in 1 mouse and RP in 3 out of 5 mice. ADC-A and docetaxel exhibits a synergistic effect. It can be concluded that ADC-A is a good treatment alone or in combination with docetaxel for the treatment of tumors resistant to docetaxel. This is all the more surprising given that the payload used has a similar mechanism of action (action on tubulin) to taxanes and therefore to docetaxel.

Claims

REVENDICATIONS
1. ADC de formule (I) suivante 1. ADC of formula (I) below
dans laquelle Ab est un anticorps anti-IGF1 R caractérisé en ce qu’il comprend des CDR de chaîne légère de séquences SEQ ID Nos. 9, 5 et 1 1 respectivement et des CDR de chaîne lourde de séquence SEQ ID Nos 7, 2 et 3 respectivement, et n est compris entre 1 et 12, in which Ab is an anti-IGF1 R antibody characterized in that it comprises light chain CDRs of sequences SEQ ID Nos. 9, 5 and 11 respectively and heavy chain CDRs of sequence SEQ ID Nos. 7, 2 and 3 respectively, and n is between 1 and 12,
pour son utilisation dans le traitement de maladies prolifératives, telle que le cancer, caractérisée en ce que l’ADC est administré de façon concomitante ou postérieurement à du docétaxel. for use in the treatment of proliferative diseases, such as cancer, characterized in that ADC is administered concomitantly or subsequently with docetaxel.
2. ADC pour son utilisation selon la revendication 1 , caractérisé en ce que Ab est un anticorps comprenant un domaine variable de chaîne légère de séquence SEQ ID No 18 et un domaine variable de chaîne lourde de séquence SEQ ID No 13. 2. ADC for its use according to claim 1, characterized in that Ab is an antibody comprising a light chain variable domain of sequence SEQ ID No 18 and a heavy chain variable domain of sequence SEQ ID No 13.
3. ADC pour son utilisation selon la revendication 1 ou 2, caractérisé en ce que l’ADC est administré à un patient ayant développé une résistance au docétaxel. 3. ADC for its use according to claim 1 or 2, characterized in that the ADC is administered to a patient who has developed resistance to docetaxel.
4. ADC pour son utilisation selon l’une quelconque des revendications 1 à 3, caractérisé en ce que le traitement par l’ADC a une durée comprise entre 1 mois et 5 ans. 4. ADC for use according to any one of claims 1 to 3, characterized in that the treatment with ADC has a duration of between 1 month and 5 years.
5. ADC pour son utilisation selon l’une quelconque des revendications 1 à 4, dans laquelle l’ADC est administré immédiatement après la constatation de la survenue de la résistance au docétaxel, ou dans les 1 , 2, 3, 4, 5, 6, 7, ou encore 8 semaines ou plus après la constatation de la survenue de la résistance, notamment avant 16 semaines suivant la constatation de la survenue de la résistance. 5. ADC for its use according to any one of claims 1 to 4, wherein ADC is administered immediately after the observation of the occurrence of resistance to docetaxel, or within 1, 2, 3, 4, 5, 6, 7, or 8 weeks or more after the onset of resistance, especially before 16 weeks after the onset of resistance.
6. ADC pour son utilisation selon l’une quelconque des revendications 1 à 5, caractérisé en ce que l’ADC est administré par cycle à une dose comprise entre 1 et 2 mg/kg de patient à traiter toutes les 2 à 4 semaines 6. ADC for its use according to any one of claims 1 to 5, characterized in that the ADC is administered per cycle at a dose of between 1 and 2 mg / kg of patient to be treated every 2 to 4 weeks
7. ADC pour son utilisation selon l’une quelconque des revendication 1 à 6, caractérisé en ce que le nombre de cycles est compris entre 1 et 18 cycles. 7. ADC for its use according to any one of claims 1 to 6, characterized in that the number of cycles is between 1 and 18 cycles.
8. ADC pour son utilisation selon l’une quelconque des revendications 1 à 7, caractérisé en ce que le traitement du cancer est mesuré par une augmentation de la survie globale, et/ou une augmentation de la durée de survie sans progression et/ou une augmentation de la survie sans aggravation et/ou une diminution de la récurrence et/ou une diminution de la taille de la tumeur. 8. ADC for its use according to any one of claims 1 to 7, characterized in that the treatment of cancer is measured by an increase in overall survival, and / or an increase in the duration of progression-free survival and / or increased survival without worsening and / or decreased recurrence and / or decreased tumor size.
9. ADC pour son utilisation selon l’une quelconque des revendication 1 à 8, caractérisé en ce que l’ADC est administré à un patient ayant été traité, préalablement ou concomitamment au docétaxel et/ ou à l’ADC, par une ou plusieurs autres chimiothérapies, notamment à l’aide d’une ou plusieurs molécules choisies dans le groupe constitué par la doxorubicine, le cyclophosphamide, la capécitabine, le cisplatine, le paclitaxel, la carboplatine, le lapatinib, le pertuzimab, le bevacizumab, le trastuzumab, le 5-fluorouracile, l’anthracycline, le binimetinib, l’encorafenib et le neratinib. 9. ADC for its use according to any one of claims 1 to 8, characterized in that the ADC is administered to a patient having been treated, before or concomitantly with docetaxel and / or with ADC, by one or more other chemotherapies, in particular using one or more molecules chosen from the group consisting of doxorubicin, cyclophosphamide, capecitabine, cisplatin, paclitaxel, carboplatin, lapatinib, pertuzimab, bevacizumab, trastuzumab, 5-fluorouracil, anthracycline, binimetinib, encorafenib and neratinib.
10. Composition pharmaceutique comprenant un ADC tel que défini selon l’une quelconque des revendications 1 et 2 et au moins un excipient pharmaceutiquement acceptable pour son utilisation dans le traitement de maladies prolifératives, telle que le cancer, caractérisée en ce que la composition pharmaceutique comprenant l’ADC est administrée de façon concomitante ou postérieurement à du docétaxel. 10. Pharmaceutical composition comprising an ADC as defined according to any one of claims 1 and 2 and at least one pharmaceutically acceptable excipient for its use in the treatment of proliferative diseases, such as cancer, characterized in that the pharmaceutical composition comprising ADC is administered concomitantly or subsequent to docetaxel.
11. Composition pharmaceutique pour son utilisation selon la revendication 10, caractérisée en ce que la maladie proliférative est un cancer résistant au docétaxel. 11. Pharmaceutical composition for its use according to claim 10, characterized in that the proliferative disease is a cancer resistant to docetaxel.
12. Composition pharmaceutique pour son utilisation selon la revendication 10 ou 11 , caractérisée en ce qu’elle est administrée immédiatement après la constatation de la survenue de la résistance au docétaxel, ou dans les 1 , 2, 3, 4, 5, 6, 7, ou encore 8 semaines ou plus après la constatation de la survenue de la résistance, notamment avant 16 semaines suivant la constatation de la survenue de la résistance. 12. Pharmaceutical composition for its use according to claim 10 or 11, characterized in that it is administered immediately after the observation of the occurrence of resistance to docetaxel, or within 1, 2, 3, 4, 5, 6, 7, or 8 weeks or more after the observation of the occurrence of resistance, in particular before 16 weeks following the observation of the occurrence of resistance.
13. Composition pharmaceutique pour son utilisation selon l’une quelconque des revendications 10 à 12, caractérisée en ce qu’elle est administrée par cycle à une dose en ADC comprise entre 1 et 2 mg/kg de patient à traiter toutes les 2 à 4 semaines, notamment avec un nombre de cycles compris entre 1 et 18 cycles. 13. Pharmaceutical composition for its use according to any one of claims 10 to 12, characterized in that it is administered per cycle at an ADC dose of between 1 and 2 mg / kg of patient to be treated every 2 to 4. weeks, especially with a number of cycles between 1 and 18 cycles.
14. Composition pharmaceutique pour son utilisation selon l’une quelconque des revendications 10 à 13, caractérisée en ce que le traitement par la composition pharmaceutique a une durée comprise entre 1 mois et 5 ans. 14. Pharmaceutical composition for its use according to any one of claims 10 to 13, characterized in that the treatment with the pharmaceutical composition has a duration of between 1 month and 5 years.
15. Composition pharmaceutique pour son utilisation selon l’une quelconque des revendications 10 à 14, caractérisée en ce que la composition pharmaceutique est administré à un patient ayant été traité, préalablement ou concomitamment au docétaxel et/ou à l’ADC, par une ou plusieurs autres chimiothérapies, notamment à l’aide d’une ou plusieurs molécules choisies dans le groupe constitué par la doxorubicine, le cyclophosphamide, la capécitabine, le cisplatine, le paclitaxel, la carboplatine, le lapatinib, le pertuzimab, le bevacizumab, le trastuzumab, le 5- fluorouracile, l’anthracycline, le binimetinib, l’encorafenib et le neratinib. 15. Pharmaceutical composition for its use according to any one of claims 10 to 14, characterized in that the pharmaceutical composition is administered to a patient who has been treated, prior to or concomitantly with docetaxel and / or ADC, with one or more several other chemotherapies, in particular using one or more molecules chosen from the group consisting of doxorubicin, cyclophosphamide, capecitabine, cisplatin, paclitaxel, carboplatin, lapatinib, pertuzimab, bevacizumab, trastuzumab , 5-fluorouracil, anthracycline, binimetinib, encorafenib and neratinib.
EP20722599.6A 2019-05-06 2020-05-06 Adc for a treatment concomitant with or subsequent to docetaxel Withdrawn EP3965822A1 (en)

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EP19305578.7A EP3735991A1 (en) 2019-05-06 2019-05-06 Adc for a concomitant or subsequent treatment with docetaxel
PCT/EP2020/062520 WO2020225282A1 (en) 2019-05-06 2020-05-06 Adc for a treatment concomitant with or subsequent to docetaxel

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EP (2) EP3735991A1 (en)
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KR (1) KR20220021456A (en)
CN (1) CN113874047A (en)
AU (1) AU2020269910A1 (en)
BR (1) BR112021021423A2 (en)
CA (2) CA3140291A1 (en)
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MA (1) MA55871A (en)
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US5595756A (en) * 1993-12-22 1997-01-21 Inex Pharmaceuticals Corporation Liposomal compositions for enhanced retention of bioactive agents
EP3134124B1 (en) 2014-04-25 2019-02-20 Pierre Fabre Medicament Igf-1r antibody-drug-conjugate and its use for the treatment of cancer
HUE047952T2 (en) * 2014-04-25 2020-05-28 Pf Medicament Antibody-drug-conjugate and its use for the treatment of cancer
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CA3140291A1 (en) 2020-11-12
US20220218838A1 (en) 2022-07-14
IL287870A (en) 2022-01-01
MA55871A (en) 2022-03-16
AU2020269910A1 (en) 2022-01-20
MX2021013596A (en) 2021-12-10
BR112021021423A2 (en) 2022-03-15
WO2020225282A8 (en) 2021-12-23
KR20220021456A (en) 2022-02-22
EP3735991A1 (en) 2020-11-11
WO2020225282A9 (en) 2022-02-10
WO2020225282A1 (en) 2020-11-12
CN113874047A (en) 2021-12-31
JP2022532555A (en) 2022-07-15

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