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HRP20131047T1 - Identifikacija antigena povezanih s tumorom za dijagnozu i lijeäśenje - Google Patents

Identifikacija antigena povezanih s tumorom za dijagnozu i lijeäśenje Download PDF

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HRP20131047T1
HRP20131047T1 HRP20131047TT HRP20131047T HRP20131047T1 HR P20131047 T1 HRP20131047 T1 HR P20131047T1 HR P20131047T T HRP20131047T T HR P20131047TT HR P20131047 T HRP20131047 T HR P20131047T HR P20131047 T1 HRP20131047 T1 HR P20131047T1
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nucleic acid
tumor
associated antigen
cancer
antibody
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HRP20131047TT
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Ugur Sahin
Özlem TÜRECI
Michael Koslowski
Dirk Usener
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Ganymed Pharmaceuticals Ag
Johannes Gutenberg-Universität Mainz, Vertreten Durch Den Präsidenten
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Publication of HRP20131047T1 publication Critical patent/HRP20131047T1/hr

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    • C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
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    • C07K14/4748—Tumour specific antigens; Tumour rejection antigen precursors [TRAP], e.g. MAGE
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    • 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
    • C07K16/30—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
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    • C12Q1/6886—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
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    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/574—Immunoassay; Biospecific binding assay; Materials therefor for cancer
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    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
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    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
    • G01N33/6854—Immunoglobulins
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Claims (22)

1. Farmaceutska kompozicija, koja sadrži jednu ili više komponenti izabranih iz grupe koju čine: (i) antitijelo koje se veže za ekstracelularni dio antigena koji je povezan sa tumorom, (ii) antisens nukleinska kiselina koja se hibridizira specifično sa nukleinskom kiselinom koja kodira antigen povezan sa tumorom, i (iii) siRNK usmjerena protiv nukleinske kiseline koja kodira antigen povezan sa tumorom, pri čemu navedeni antigen povezan sa tumorom ima sekvencu kodiranu nukleinskom kiselinom koja je izabrana iz grupe koju čine: (a) nukleinska kiselina koja sadrži nukleinsko kiselinsku sekvencu SEQ ID NO: 1, (b) nukleinska kiselina koja hibridizira sa nukleinskom kiselinom iz (a) pod vrlo specifičnim uvjetima, (c) nukleinska kiselina koja je degenerirana s obzirom na nukleinsku kiselinu pod (a) ili (b), i (d) nukleinska kiselina koja je najmanje 95% identična sa nukleinskom kiselinom pod (a), (b) ili (c) za uporabu u postupku za liječenje ili prevenciju kancera naznačenog ekspresijom antigena koji je povezan sa tumorom.
2. Farmaceutska kompozicija prema patentnom zahtjevu 1 za uporabu u postupku za liječenje ili prevenciju kancera naznačenog ekspresijom antigena povezanog sa tumorom prema patentnom zahtjevu 1, gdje je antitijelo monoklonalno, himerno ili humanizirano antitijelo, ili je fragment antitijela.
3. Farmaceutska kompozicija prema patentnom zahtjevu 1 ili 2 za uporabu u postupku za liječenje ili prevenciju kancera naznačenog ekspresijom antigena povezanog sa tumorom prema patentnom zahtjevu 1, gdje je antitijelo spojeno za terapeutsko ili dijagnostičko sredstvo.
4. Farmaceutska kompozicija prema bilo kojem od patentnih zahtjeva 1-3 za uporabu u postupku za liječenje ili prevenciju kancera naznačenog ekspresijom antigena povezanog sa tumorom prema patentnom zahtjevu 1, gdje je kancer – tumor pluća, tumor dojke, tumor prostate, melanom, tumor debelog crijeva, tumor želuca, tumor pankreasa, ORL tumor, karcinom renalnih stanica ili karcinom grlića materice, karcinom debelog crijeva ili karcinom dojke.
5. Farmaceutska kompozicija prema bilo kojem od patentnih zahtjeva 1-4 za uporabu u postupku za liječenje ili prevenciju kancera naznačenog ekspresijom antigena povezanog sa tumorom prema patentnom zahtjevu 1, gdje antigen povezan sa tumorom sadrži aminokiselinsku sekvencu izabranu iz grupe koju čine SEQ ID NOs: 2 i 7-11.
6. In vitro postupak za dijagnostificiranje ili praćenje bolesti kancera naznačene ekspresijom antigena povezanog sa tumorom, pri čemu taj postupak sadrži detekciju ili određivanje količine (i) nukleinske kiseline koja kodira antigen povezan sa tumorom, i/ili (ii) antigena povezanog sa tumorom, u biološkom uzorku izoliranom iz pacijenta, pri čemu navedeni antigen povezan sa tumorom ima sekvencu koju kodira nukleinska kiselina koja je izabrana iz grupe koju čine: (a) nukleinska kiselina koja sadrži nukleinsko kiselinsku sekvencu SEQ ID NO: 1, (b) nukleinska kiselina koja hibridizira sa nukleinskom kiselinom iz (a) pod vrlo specifičnim uvjetima, (c) nukleinska kiselina koja je degenerirana s obzirom na nukleinsku kiselinu pod (a) ili (b), i (d) nukleinska kiselina koja je najmanje 95% identična sa nukleinskom kiselinom pod (a), (b) ili (c).
7. Postupak prema patentnom zahtjevu 6, u kojem detekcija ili određivanje količine sadrži (i) dovođenje u kontakt biološkog uzorka sa sredstvom koje se vezuje specifično za nukleinsku kiselinu koja kodira antigen povezan sa tumorom ili za navedeni antigen povezan sa tumorom i (ii) detekciju formiranja ili određivanje količine kompleksa između sredstva i nukleinske kiseline ili antigena koji je povezan sa tumorom.
8. Postupak prema patentnom zahtjevu 7, naznačen time što je sredstvo koje se vezuje specifično za nukleinsku kiselinu koja kodira antigen povezan sa tumorom – oligonukleotid ili polinukleotid, koji specifično hibridizira sa navedenom nukleinskom kiselinom.
9. Postupak prema patentnom zahtjevu 7, naznačen time što je sredstvo koje se vezuje specifično za antigen povezan sa tumorom - antitijelo koje se specifično veže za navedeni antigen povezan sa tumorom.
10. Postupak prema bilo kojem od patentnih zahtjeva 6 do 9 naznačen time što navedeno praćenje navedene bolesti kancera sadrži određivanje regresije, toka ili početka navedene bolesti u uzorku od pacijenta koji ima navedenu bolest ili za koga se sumnja da se razboljeva od navedene bolesti.
11. Postupak prema patentnom zahtjevu 10, naznačen time što sadrži detekciju ili određivanje količine u prvom uzorku u prvoj vremenskoj točki i u drugom uzorku u drugoj vremenskoj točki i usporedbu dva uzorka.
12. Postupak prema bilo kojem od patentnih zahtjeva 7-11, naznačen time što je sredstvo obilježeno na detektabilni način.
13. Postupak prema bilo kojem od patentnih zahtjeva 6-12, naznačen time što uzorak sadrži tjelesnu tekućinu i/ili tjelesno tkivo.
14. Postupak prema bilo kojem od patentnih zahtjeva 6-13, naznačen time što antigen povezan sa tumorom sadrži aminokiselinsku sekvencu izabranu iz grupe koju čine SEQ ID NOs: 2 i 7-11.
15. Antitijelo za uporabu u postupku za liječenje, prevenciju, dijagnostificiranje ili praćenje bolesti kancera naznačene ekspresijom antigena povezanog sa tumorom, pri čemu navedeni antigen povezan sa tumorom ima sekvencu kodiranu od strane nukleinske kiseline koja je izabrana iz grupe koju čine: (a) nukleinska kiselina koja sadrži nukleinsko kiselinsku sekvencu SEQ ID NO: 1, (b) nukleinska kiselina koja hibridizira sa nukleinskom kiselinom iz (a) pod vrlo specifičnim uvjetima, (c) nukleinska kiselina koja je degenerirana s obzirom na nukleinsku kiselinu pod (a) ili (b), i (d) nukleinska kiselina koja je najmanje 95% identična sa nukleinskom kiselinom pod (a), (b) ili (c), pri čemu se antitijelo vezuje za ekstracelularni dio navedenog antigena povezanog sa tumorom i spojeno je sa terapeutskim ili dijagnostičkim sredstvom.
16. Antitijelo prema patentnom zahtjevu 15 za uporabu u postupku za liječenje, prevenciju, dijagnostificiranje ili praćenje bolesti kancera naznačene ekspresijom antigena povezanog sa tumorom prema patentnom zahtjevu 15, koje je monoklonalno, himerno ili humanizirano antitijelo, ili je fragment antitijela.
17. Antitijelo prema patentnom zahtjevu 15 ili 16 za uporabu u postupku za liječenje, prevenciju, dijagnostificiranje ili praćenje bolesti kancera naznačene ekspresijom antigena povezanog sa tumorom prema patentnom zahtjevu 15, pri čemu antigen povezan sa tumorom sadrži aminokiselinsku sekvencu izabranu iz grupe koju čine SEQ ID NOs: 2 i 7-11.
18. Antitijelo prema bilo kojem od patentnih zahtjeva 15, 16 ili 17 za uporabu u postupku za liječenje, prevenciju, dijagnostificiranje ili praćenje bolesti kancera naznačene ekspresijom antigena povezanog sa tumorom prema patentnom zahtjevu 15, u kojem je terapeutsko ili dijagnostičko sredstvo – toksin.
19. Farmaceutska kompozicija prema bilo kojem od patentnih zahtjeva 1-5 za uporabu u postupku za liječenje ili prevenciju kancera naznačenog ekspresijom antigena povezanog sa tumorom prema patentnom zahtjevu 1 za inhibiciju razvoja kancera kod pacijenta, pri čemu se farmaceutska kompozicija primjenjuje u efikasnoj količini.
20. Konjugat između antitijela i terapeutskog ili dijagnostičkog sredstva, gdje se antitijelo veže specifično za ekstracelularni dio proteina ili polipeptida, pri čemu je navedeni protein ili polipeptid kodiran od strane nukleinske kiseline izabrane iz grupe koju čine: (a) nukleinska kiselina koja sadrži nukleinsko kiselinsku sekvencu SEQ ID NO: 1, (b) nukleinska kiselina koja hibridizira sa nukleinskom kiselinom iz (a) pod vrlo specifičnim uvjetima, (c) nukleinska kiselina koja je degenerirana s obzirom na nukleinsku kiselinu pod (a) ili (b), i (d) nukleinska kiselina koja je najmanje 95% identična sa nukleinskom kiselinom pod (a), (b) ili (c) za uporabu u liječenju, prevenciji, dijagnostificiranju ili praćenju bolesti kancera naznačene ekspresijom proteina ili polipeptida.
21. Konjugat prema patentnom zahtjevu 20 za uporabu u postupku za liječenje, prevenciju, dijagnostificiranje ili praćenje bolesti kancera naznačene ekspresijom proteina ili polipeptida prema patentnom zahtjevu 20, u kojem je terapeutsko ili dijagnostičko sredstvo - toksin.
22. Uporaba kompleta za in vitro dijagnostificiranje bolesti kancera naznačene ekspresijom antigena povezanog sa tumorom, pri čemu komplet sadrži sredstva za detekciju ili određivanje količine (i) nukleinske kiseline koja kodira antigen povezan sa tumorom, i/ili (ii) antigena povezanog sa tumorom, u biološkom uzorku izoliranom iz pacijenta, pri čemu navedeni antigen povezan sa tumorom ima sekvencu koju kodira nukleinska kiselina koja je izabrana iz grupe koju čine: (a) nukleinska kiselina koja sadrži nukleinsko kiselinsku sekvencu SEQ ID NO: 1, (b) nukleinska kiselina koja hibridizira sa nukleinskom kiselinom iz (a) pod vrlo specifičnim uvjetima, (c) nukleinska kiselina koja je degenerirana s obzirom na nukleinsku kiselinu pod (a) ili (b), i (d) nukleinska kiselina koja je najmanje 95% identična sa nukleinskom kiselinom pod (a), (b) ili (c).
HRP20131047TT 2005-09-12 2006-09-06 Identifikacija antigena povezanih s tumorom za dijagnozu i lijeäśenje HRP20131047T1 (hr)

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EP20050019786 EP1762575A1 (en) 2005-09-12 2005-09-12 Identification of tumor-associated antigens for diagnosis and therapy
PCT/EP2006/008695 WO2007031222A2 (en) 2005-09-12 2006-09-06 Identification of tumor-associated antigens for diagnosis and therapy

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HRP20131047T1 true HRP20131047T1 (hr) 2013-12-06

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HRP20150432TT HRP20150432T1 (hr) 2005-09-12 2015-04-21 Indentifikacija antigena povezanih s tumorom za dijagnozu i terapiju
HRP20180507TT HRP20180507T1 (hr) 2005-09-12 2018-03-27 Identifikacija antigena povezanih s tumorom za dijagnozu i terapiju

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