| CPC C07K 16/2878 (2013.01) [A61K 39/395 (2013.01); A61P 35/00 (2018.01); C07K 16/18 (2013.01); C07K 16/2809 (2013.01); C07K 2317/21 (2013.01); C07K 2317/24 (2013.01); C07K 2317/31 (2013.01); C07K 2317/56 (2013.01); C07K 2317/565 (2013.01); C07K 2317/569 (2013.01); C07K 2317/622 (2013.01); C07K 2317/732 (2013.01); C07K 2317/76 (2013.01); C07K 2317/92 (2013.01); C07K 2319/30 (2013.01); C07K 2319/31 (2013.01)] | 25 Claims |
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1. A method for treating a cancer in a human subject having the cancer, comprising administering to the subject a pharmaceutical composition comprising a B cell maturation agent (BCMA) binding trispecific protein that comprises:
(a) a first domain (A) which is a single chain variable fragment (scFv) that specifically binds to a human CD3ε;
(b) a second domain (B) which is a single domain antibody that specifically binds to a human serum albumin protein; and
(c) a third domain (C) which is a single domain antibody that specifically binds to a human BCMA comprising the sequence of SEQ ID NO: 468,
wherein the third domain comprises complementarity determining regions CDR1, CDR2, and CDR3,
wherein the CDR1 comprises the amino acid sequence of SEQ ID NO: 76, the CDR2 comprises the amino acid sequence of SEQ ID NO: 190, and the CDR3 comprises the amino acid sequence of SEQ ID NO: 304, and
wherein the cancer expresses BCMA.
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