HRP20171758T1 - Kombinacija dr5 agonista i anti-pd-1 antagonista i načini primjene - Google Patents

Kombinacija dr5 agonista i anti-pd-1 antagonista i načini primjene Download PDF

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HRP20171758T1
HRP20171758T1 HRP20171758TT HRP20171758T HRP20171758T1 HR P20171758 T1 HRP20171758 T1 HR P20171758T1 HR P20171758T T HRP20171758T T HR P20171758TT HR P20171758 T HRP20171758 T HR P20171758T HR P20171758 T1 HRP20171758 T1 HR P20171758T1
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antagonist
agonist
cancer
use according
antigen
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Bryan BARNHART
Maria N. Jure-Kunkel
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Bristol-Myers Squibb Company
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    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2803Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
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    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2803Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
    • C07K16/2827Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against B7 molecules, e.g. CD80, CD86
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    • C07ORGANIC CHEMISTRY
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    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2878Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the NGF-receptor/TNF-receptor superfamily, e.g. CD27, CD30, CD40, CD95
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K39/00Medicinal preparations containing antigens or antibodies
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    • C07K2317/569Single domain, e.g. dAb, sdAb, VHH, VNAR or nanobody®

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Claims (24)

1. PD-1 antagonista i DR5 agonista za primjenu u metodi za liječenje raka, gdje PD-1 antagonista je anti-PD-1 antitijelo ili njegov antigen-vezujući fragment, i DR5 agonista je anti-DR5 antitijelo ili njegov antigen-vezujući fragment
2. PD-1 antagonista za primjenu u metodi za liječenje raka, gdje metoda dalje sadrži administraciju DR5 agonista, gdje PD-1 antagonista je anti-PD-1 antitijelo ili njegov antigen-vezujući fragment, i DR5 agonista je anti-DR5 antitijelo ili njegov antigen-vezujući fragment
3. DR5 agonista za primjenu u metodi za liječenje raka, gdje metoda dalje sadrži administraciju PD-1 antagonista, gdje PD-1 antagonista je anti-PD-1 antitijelo ili njegov antigen-vezujući fragment, i DR5 agonista je anti-DR5 antitijelo ili njegov antigen-vezujući fragment
4. PD-1 antagonista i/ili DR5 agonista za primjenu prema bilo kojem od patentnih zahtjeva 1-3, gdje DR5 agonista je odabran od Leksatumumaba, Tigatuzumaba, Konatumumaba, Drozitumaba, HGSTR2J/KMTRS, i LBY-135.
5. PD-1 antagonista i/ili DR5 agonista za primjenu prema bilo kojem od patentnih zahtjeva 1-4, gdje PD-1 antagonista sadrži CDR1, CDR2 i CDR3 domene u varijabilnoj regiji teškog lanca koji ima sekvencu prikazanu u SEQ ID NO: 13, i CDR1, CDR2 i CDR3 domene u varijabilnoj regiji lakog lanca koji ima sekvencu prikazanu u SEQ ID NO: 15.
6. PD-1 antagonista i/ili DR5 agonista za primjenu prema bilo kojem od patentnih zahtjeva 1-5, gdje PD-1 antagonista sadrži: (a) CDR1 varijabilne regije teškog lanca koji ima sekvencu prikazanu u SEQ ID NO: 17; (b) CDR2 varijabilne regije teškog lanca koji ima sekvencu prikazanu u SEQ ID NO: 18; (c) CDR3 varijabilne regije teškog lanca koja ima sekvencu prikazanu u SEQ ID NO: 19; (d) CDR1 varijabilne regije lakog lanca koji ima sekvencu prikazanu u SEQ ID NO: 20; (e) CDR 2 varijabilne regije lakog lanca koji ima sekvencu prikazanu u SEQ ID NO: 21; i (f) CDR 3 varijabilne regije lakog lanca koji ima sekvencu prikazanu u SEQ ID NO: 22.
7. PD-1 antagonista i/ili DR5 agonista za primjenu prema bilo kojem od patentnih zahtjeva 1-5, gdje PD-1 antagonista sadrži varijabilne regije teških i lakih lanaca koji imaju sekvence prikazane u SEQ ID NOs: 13 i 15, redom.
8. PD-1 antagonista i/ili DR5 agonista za primjenu prema bilo kojem od patentnih zahtjeva 1-5, gdje PD-1 antagonista sadrži teške i lake lance koji imaju sekvence prikazane u SEQ ID NOs: 11 i 12, redom.
9. PD-1 antagonista i/ili DR5 agonista za primjenu prema bilo kojem od patentnih zahtjeva 1-8, gdje administracija PD-1 antagonista i DR5 agonista smanjuje veličinu tumora za najmanje 50%.
10. PD-1 antagonista i/ili DR5 agonista za primjenu prema bilo kojem od patentnih zahtjeva 1-8, gdje administracija PD-1 antagonista i DR5 agonista, smanjuje veličinu tumora za najmanje 80%.
11. PD-1 antagonista i/ili DR5 agonista za primjenu prema bilo kojem od patentnih zahtjeva 1-8, gdje administracija PD-1 antagonista i DR5 agonista dovodi do inhibicije rasta tumora od najmanje 80%.
12. PD-1 antagonista i/ili DR5 agonista za primjenu prema bilo kojem od patentnih zahtjeva 1-8, gdje liječenje proizvodi najmanje jedan terapijski efekt izabran od smanjenja veličine tumora, smanjenja broja metastatskih lezija tijekom vremena, kompletnog odgovora, djelomičnog odgovora i stabilne bolesti.
13. PD-1 antagonista i/ili DR5 agonista za primjenu prema bilo kojem od patentnih zahtjeva 1-12, gdje PD-1 antagonista i DR5 agonista su formulirani za intravensku administraciju.
14. PD-1 antagonista i/ili DR5 agonista za primjenu prema bilo kojem od patentnih zahtjeva 1-12, gdje metoda sadrži administriranje PD-1 antagonista prije administriranja DR5 agonista.
15. PD-1 antagonista i/ili DR5 agonista za primjenu prema bilo kojem od patentnih zahtjeva 1-12, gdje metoda sadrži administriranje DR5 agonista prije administriranja PD-1 antagonista.
16. PD-1 antagonista i/ili DR5 agonista za primjenu prema bilo kojem od patentnih zahtjeva 1-12, gdje metoda sadrži administriranje DR5 agonista i PD-1 antagonista istovremeno.
17. PD-1 antagonista i/ili DR5 agonista za primjenu prema bilo kojem od patentnih zahtjeva 1-16, gdje rak je rak odabran od leukemije, limfoma, blastoma, karcinoma i sarkoma.
18. PD-1 antagonista i/ili DR5 agonista za primjenu prema bilo kojem od patentnih zahtjeva 1-16, gdje je rak odabran od kronične mijeloične leukemije, akutne limfoblastična leukemije, akutne limfoblastične leukemije pozitivne na Philadelphia kromosom (Ph+ ALL), karcinoma skvamoznih stanica, sitnostaničnog raka pluća, nesitnostaničnog raka pluća, glioma, gastrointestinalnog raka, raka bubrega, raka jajnika, raka jetre, kolorektalnog raka, raka endometrija, raka bubrega, raka prostate, raka štitnjače, neuroblastoma, raka gušterače, glioblastoma multiforme, raka grlića maternice, raka trbuha, raka mokraćnog mjehura, hepatoma, raka dojke, raka debelog crijeva, raka glave i vrata, raka želuca, tumora zametnih stanica, pedijatrijskog sarkoma, sinonasalnog prirodnog ubojice, multiplog mijeloma, akutne mijelogene leukemije (AML), i kronične limfocitne leukemije (CML).
19. PD-1 antagonista i/ili DR5 agonista za primjenu prema bilo kojem od patentnih zahtjeva 1-18, gdje metoda za liječenje raka dalje sadrži administraciju dodatnog terapijskog agensa.
20. PD-1 antagonista i/ili DR5 agonista za primjenu prema patentnom zahtjevu 19, gdje dodatni terapijski agens je citotoksin ili kemoterapijski agens.
21. PD-1 antagonista i/ili DR5 agonista za primjenu prema bilo kojem od patentnih zahtjeva 1-20, gdje subjekt koga treba liječiti je čovjek.
22. Kompozicija koja sadrži PD-1 antagonistu i DR5 agonistu, gdje PD-1 antagonista je anti-PD-1 antitijelo ili njegov antigen-vezujući fragment, i DR5 agonista je anti-DR5 antitijelo ili njegov antigen-vezujući fragment.
23. Kompozicija iz patentnog zahtjeva 22 za primjenu u metodi za liječenje raka.
24. Set za liječenje raka kod subjekta, set koji sadrži: (a) dozu PD-1 antagonista; (b) dozu DR5 agonista; i (c) instrukcije za primjenu PD-1 antagonista i DR5 agonista prema bilo kojem od patentnih zahtjeva 1-23, gdje PD-1 antagonista je anti-PD-1 antitijelo ili njegov antigen-vezujući fragment, i DR5 agonista je anti-DR5 antitijelo ili njegov antigen-vezujući fragment.
HRP20171758TT 2013-03-14 2017-11-14 Kombinacija dr5 agonista i anti-pd-1 antagonista i načini primjene HRP20171758T1 (hr)

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US201361783184P 2013-03-14 2013-03-14
EP14717294.4A EP2970473B1 (en) 2013-03-14 2014-03-12 Combination of dr5 agonist and anti-pd-1 antagonist and methods of use
PCT/US2014/024208 WO2014159562A1 (en) 2013-03-14 2014-03-12 Combination of dr5 agonist and anti-pd-1 antagonist and methods of use

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EP (2) EP3305812B1 (hr)
CY (1) CY1119510T1 (hr)
DK (1) DK2970473T3 (hr)
ES (2) ES2812208T3 (hr)
HR (1) HRP20171758T1 (hr)
HU (1) HUE035865T2 (hr)
LT (1) LT2970473T (hr)
ME (1) ME02917B (hr)
NO (1) NO3080374T3 (hr)
PL (1) PL2970473T3 (hr)
PT (1) PT2970473T (hr)
RS (1) RS56531B1 (hr)
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