HRP20161194T1 - Anti-bcma protutijela - Google Patents

Anti-bcma protutijela Download PDF

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HRP20161194T1
HRP20161194T1 HRP20161194TT HRP20161194T HRP20161194T1 HR P20161194 T1 HRP20161194 T1 HR P20161194T1 HR P20161194T T HRP20161194T T HR P20161194TT HR P20161194 T HRP20161194 T HR P20161194T HR P20161194 T1 HRP20161194 T1 HR P20161194T1
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seq
variable domain
chain variable
antibody
antigen
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HRP20161194TT
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Susan L. Kalled
Yen-Ming Hsu
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Biogen Ma Inc.
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Publication of HRP20161194T1 publication Critical patent/HRP20161194T1/hr

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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
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Claims (16)

1. Izolirano protutijelo ili njegov antigen-vezujući fragment koji se veže za polipeptid SEQ ID NO:9, pri čemu protutijelo ili njegov antigen-vezujući fragment sadrže: a) varijabilnu domenu teškog lanca koja sadrži CDR1 regiju koja sadrži aminokiseline 31-35 iz SEQ ID NO:3, CDR2 regiju koja sadrži aminokiseline 50-66 iz SEQ ID NO:3 i CDR3 regiju koja sadrži aminokiseline 99-106 iz SEQ ID NO:3; i varijabilnu domenu lakog lanca koja sadrži CDR1 regiju koja sadrži aminokiseline 24-38 iz bilo kojeg od SEQ ID NO: 4, 11 ili 12, CDR2 regiju koja sadrži aminokiseline 54-60 iz bilo kojeg od SEQ ID NO: 4, 11 ili 12 i CDR3 regiju koja sadrži aminokiseline 93-101 iz bilo kojeg odSEQ ID NO: 4, 11 ili 12; b) varijabilnu domenu teškog lanca koja sadrži CDR1 regiju koja sadrži aminokiseline 31-35 iz SEQ ID NO:5, CDR2 regiju koja sadrži aminokiseline 50-66 iz SEQ ID NO:5 i CDR3 regiju koja sadrži aminokiseline 99-106 iz SEQ ID NO:5; i varijabilnu domenu lakog lanca koja sadrži CDR1 regiju koja sadrži aminokiseline 24-38 iz SEQ ID NO: 6, CDR2 regiju koja sadrži aminokiseline 54-60 iz SEQ ID NO: 6 i CDR3 regiju koja sadrži aminokiseline 93-101 iz SEQ ID NO: 6; ili c) varijabilnu domenu teškog lanca koja sadrži CDR1 regiju koja sadrži aminokiseline 31-35 iz SEQ ID NO:7, CDR2 regiju koja sadrži aminokiseline 50-66 iz SEQ ID NO:7 i CDR3 regiju koja sadrži aminokiseline 99-106 iz SEQ ID NO:7; i varijabilnu domenu lakog lanca koja sadrži CDR1 regiju koja sadrži aminokiseline 24-38 iz SEQ ID NO: 8, CDR2 regiju koja sadrži aminokiseline 54-60 iz SEQ ID NO: 8 i CDR3 regiju koja sadrži aminokiseline 93-101 iz SEQ ID NO: 8.
2. Protutijelo ili antigen-vezujući fragment iz patentnog zahtjeva 1, pri čemu protutijelo ili antigen-vezujući fragment sadrži: a) varijabilnu domenu teškog lanca koja sadrži SEQ ID NO: 3 i varijabilnu domenu lakog lanca koja sadrži SEQ ID NO: 12; b) varijabilnu domenu teškog lanca koja sadrži SEQ ID NO: 3 i varijabilnu domenu lakog lanca koja sadrži SEQ ID NO: 4; c) varijabilnu domenu teškog lanca koja sadrži SEQ ID NO: 3 i varijabilnu domenu lakog lanca koja sadrži SEQ ID NO: 11; d) varijabilnu domenu teškog lanca koja sadrži SEQ ID NO: 5 i varijabilnu domenu lakog lanca koja sadrži SEQ ID NO: 6; ili e) varijabilnu domenu teškog lanca koja sadrži SEQ ID NO: 7 i varijabilnu domenu lakog lanca koja sadrži SEQ ID NO: 8.
3. Protutijelo ili antigen-vezujući fragment iz patentnog zahtjeva 1, pri čemu protutijelo ili antigen-vezujući fragment sadrži: a) teški lanac koji sadrži SEQ ID NO: 15 i laki lanac koji sadrži SEQ ID NO: 16 ili SEQ ID NO: 17; b) teški lanac koji sadrži SEQ ID NO: 18 i laki lanac koji sadrži SEQ ID NO: 19; ili c) teški lanac koji sadrži SEQ ID NO: 20 i laki lanac koji sadrži SEQ ID NO: 21.
4. Protutijelo ili antigen-vezujući fragment iz patentnog zahtjeva 1, pri čemu protutijelo ili antigen-vezujući fragment sadrži: a) varijabilnu domenu teškog lanca koja sadrži slijed koji je najmanje 95% identičan slijedu odabranom između SEQ ID NO: 25-29 i varijabilnu domenu lakog lanca koja sadrži slijed koji je najmanje 95% identičan slijedu odabranom između SEQ ID NO: 22-24; b) varijabilnu domenu teškog lanca koja sadrži slijed koji je najmanje 95% identičan slijedu odabranom između SEQ ID NO: 34-38 i varijabilnu domenu lakog lanca koja sadrži slijed koji je najmanje 95% identičan slijedu odabranom između SEQ ID NO: 30-33; ili c) varijabilnu domenu teškog lanca koja sadrži slijed koji je najmanje 95% identičan slijedu odabranom između SEQ ID NO: 43-47 i varijabilnu domenu lakog lanca koja sadrži slijed koji je najmanje 95% identičan slijedu odabranom između SEQ ID NO: 39-42.
5. Protutijelo ili antigen-vezujući fragment iz patentnog zahtjeva 4, pri čemu protutijelo ili antigen-vezujući fragment sadrži: a) varijabilnu domenu teškog lanca koja sadrži bilo koju od SEQ ID NO: 25-29 i varijabilnu domenu lakog lanca koja sadrži bilo koju od SEQ ID NO: 22-24; b) varijabilnu domenu teškog lanca koja sadrži SEQ ID NO: 34-38 i varijabilnu domenu lakog lanca koja sadrži SEQ ID NO: 30-33; ili c) varijabilnu domenu teškog lanca koja sadrži SEQ ID NO: 43-47 i varijabilnu domenu lakog lanca koja sadrži SEQ ID NO: 39-42.
6. Protutijelo iz bilo kojeg od patentnih zahtjeva 1-2, pri čemu je protutijelo kimerno ili jednolančano protutijelo.
7. Protutijelo iz patentnog zahtjeva 1, pri čemu je protutijelo humanizirano protutijelo.
8. Polipeptid koji se veže za SEQ ID NO:9 i sadrži antigen-vezni dio, Fab fragment, ili F(ab')2 fragment protutijela iz bilo kojeg od patentnih zahtjeva 1-7.
9. Hibridoma koja stvara protutijelo iz bilo kojeg od patentnih zahtjeva 1-7.
10. Farmaceutski sastav koji sadrži: a) protutijelo ili antigen-vezujući fragment iz bilo kojeg od patentnih zahtjeva 1-7; ili b) polipeptid iz patentnog zahtjeva 8.
11. Protutijelo ili antigen-vezujući fragment iz bilo kojeg od patentnih zahtjeva 1-7 za uporabu u liječenju poremećaja povezanog s B-stanicama.
12. Protutijelo ili antigen-vezujući fragment za uporabu kao u patentnom zahtjevu 11, gdje je poremećaj povezan s B-stanicama plazmocitom, Hodgkinov limfom, folikularni limfom, limfom mailh nezarezanih stanica, endemski Burkittov limfom, sporadični Burkitov limfom, limfom marginalne zone, ekstranodalni limfom limfoidnog tkiva povezanog s mukozom, nodalni monocitoidni B-stanični limfom, limfom slezene, limfom plaštenih stanica, limfom velikih stanica, difuzni limfom miješanih stanica, imunoblastični limfom, primarni medijastinalni B-stanični limfom, plućni B-stanični angiocentrični limfom, limfom malih limfocita, B-stanične proliferacije nepoznatog malignog potencijala, limfomatoidna granulomatoza, post-transplantacijski limfoproliferativni poremećaj, imunoregulatorni poremećaj, reumatoidni artritis, mijastenija gravis, idiopatska trombocitopenična purpura, antifosfolipidni sindrom, Chagasova bolest, Graveova bolest, Wegenerova granulomatoza, poliarteritis nodoza, Sjogrenov sindrom, obični pemfigus, skleroderma, multipla skleroza, antifosfolipidni sindrom, vaskulitis povezan s ANCA-om, Goodpasteureova bolest, Kawasakijeva bolest, autoimuna hemolitička anemija, brzoprogredirajući glomerulonefritis, bolest teških lanaca, primarna ili s imunocitima povezana amiloidoza, ili monoklonska gamopatija neodređenog značenja.
13. Protutijelo ili antigen-vezujući fragment za uporabu kao u patentnom zahtjevu 12, gdje je poremećaj povezan s B-stanicama a) malignitet B-stanica, kao što je malignitet plazma stanica; b) autoimuna bolest; c) idiopatska trombocitopenična purpura; d) mijastenija gravis; ili e) autoimuna hemolitička anemija.
14. Protutijelo ili antigen-vezujući fragment za uporabu kao u patentnom zahtjevu 13, gdje je malignitet plazma stanica multipli mijelom.
15. Protutijelo ili antigen-vezujući fragment za uporabu kao u patentnom zahtjevu 13, gdje je autoimuna bolest sustavni eritematozni lupus ili reumatoidni artritis.
16. Protutijelo ili antigen-vezujući fragment za uporabu kao u patentnom zahtjevu 11 ili 12, gdje se protutijelo ili antigen-vezujući fragment daju zajedno s RITUXAN-om.
HRP20161194TT 2009-03-10 2016-09-19 Anti-bcma protutijela HRP20161194T1 (hr)

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US15894209P 2009-03-10 2009-03-10
US16292409P 2009-03-24 2009-03-24
EP10708865.0A EP2406284B9 (en) 2009-03-10 2010-03-10 Anti-bcma antibodies
PCT/US2010/026825 WO2010104949A2 (en) 2009-03-10 2010-03-10 Anti-bcma antibodies

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CN (2) CN102421801B (hr)
AU (2) AU2010224160A1 (hr)
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