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PE20130528A1 - PROTEINAS QUE SE UNEN AL TNF-alfa - Google Patents

PROTEINAS QUE SE UNEN AL TNF-alfa

Info

Publication number
PE20130528A1
PE20130528A1 PE2012002003A PE2012002003A PE20130528A1 PE 20130528 A1 PE20130528 A1 PE 20130528A1 PE 2012002003 A PE2012002003 A PE 2012002003A PE 2012002003 A PE2012002003 A PE 2012002003A PE 20130528 A1 PE20130528 A1 PE 20130528A1
Authority
PE
Peru
Prior art keywords
alpha
seq
tnf
region
protein
Prior art date
Application number
PE2012002003A
Other languages
English (en)
Inventor
Lorenzo Benatuil
Tariq Ghayur
Carrie L Goodreau
Peter C Isakson
Jochen Salfeld
Original Assignee
Abbvie Inc
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=44761064&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20130528(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Abbvie Inc filed Critical Abbvie Inc
Publication of PE20130528A1 publication Critical patent/PE20130528A1/es

Links

Classifications

    • 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
    • C07K16/24—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
    • C07K16/241—Tumor Necrosis Factors
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    • A61K47/00—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
    • 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
    • A61K47/6845—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 cytokine, e.g. growth factors, VEGF, TNF, a lymphokine or an interferon
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    • A61K51/02—Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
    • A61K51/04—Organic compounds
    • A61K51/08—Peptides, e.g. proteins, carriers being peptides, polyamino acids, proteins
    • A61K51/10—Antibodies or immunoglobulins; Fragments thereof, the carrier being an antibody, an immunoglobulin or a fragment thereof, e.g. a camelised human single domain antibody or the Fc fragment of an antibody
    • A61K51/1021—Antibodies or immunoglobulins; Fragments thereof, the carrier being an antibody, an immunoglobulin or a fragment thereof, e.g. a camelised human single domain antibody or the Fc fragment of an antibody against cytokines, e.g. growth factors, VEGF, TNF, lymphokines or interferons
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Abstract

SE REFIERE A UNA PROTEINA DE UNION HUMANIZADA CARACTERIZADA POR: UN DOMINIO DE UNION AL ANTIGENO QUE SE UNE AL FACTOR DE NECROSIS TUMORAL-ALFA HUMANO(TNF-ALFA), QUE COMPRENDE UNA REGION VH QUE PRESENTA SEQ ID Nº 24,25,28- 33 Y UNA REGION VL QUE COMPRENDE SEQ ID Nº 26, 27, 34-36. LA REGION CONSTANTE DEL DOMINIO DE LA CADENA PESADA DE LA INMUNOGLOBULINA ES UN DOMINIO CONSTANTE DE LA IgG1 HUMANA QUE COMPRENDE SEQ ID Nº 2 O SEQ ID Nº 3. DICHA PROTEINA MODULA, NEUTRALIZA Y DISMINUYE LA CAPACIDAD DEL TNF-? DE UNIRSE ASU RECEPTOR. REFERIDA ADEMAS A UNA COMPOSICION FARMACEUTICA. DICHA PROTEINA ES UTIL COMO AGENTE PARA EL DIAGNOSTICO POR IMAGENES, AGENTE TERAPEUTICO O UN AGENTE CITOTOXICO ENTRE OTROS, DONDE SE PRESENTA TRANSTORNOS DE LA ACTIVIDAD DE LA TNF-ALFA.
PE2012002003A 2010-04-07 2011-04-06 PROTEINAS QUE SE UNEN AL TNF-alfa PE20130528A1 (es)

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UY33319A (es) 2011-12-01
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