| CPC A61K 47/641 (2017.08) [A61K 47/547 (2017.08); A61K 51/0495 (2013.01); A61K 51/10 (2013.01); A61K 51/1096 (2013.01); C07K 14/4746 (2013.01); C07K 14/7155 (2013.01); C07K 16/3084 (2013.01); C07K 16/44 (2013.01); C07K 2317/622 (2013.01); C07K 2317/92 (2013.01); C07K 2317/94 (2013.01); C07K 2319/70 (2013.01)] | 11 Claims |
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1. A method of treating or diagnosing cancer in a subject, comprising:
a. providing a composition comprising a conjugate comprising a self-assembly disassembly (SADA) polypeptide having an amino acid sequence that is identical to a human homo-multimerizing polypeptide sequence comprising any one of SEQ ID NOs: 1, 3, 5, 7, 9, 11, 13, and 15 and having one or more multimerization dissociation constants (KD); and a bispecific antibody comprising a first scFv that binds a tumor target and a second scFv that binds a DOTA moiety comprising a radioactive payload, wherein (a) the first scFv is operably linked to the second scFv, (b) the second scFv includes a VH-CDR1 sequence comprising DYGVH (SEQ ID NO: 103), a VH-CDR2 sequence comprising VIWSGGGTAYNTALIS (SEQ ID NO: 104), a VH-CDR3 sequence comprising RGSYPYNYFDA (SEQ ID NO: 105), a VL-CDR1 sequence comprising GSSTGAVTASNYAN (SEQ ID NO: 106), a VL-CDR2 sequence comprising GHNNRPP (SEQ ID NO: 107), and a VH-CDR3 sequence comprising ALWYSDHWV (SEQ ID NO: 108); and (c) the second scFv is operably linked to the SADA polypeptide;
b. administering the composition to a subject that is suffering from or susceptible to cancer; and
c. administering a DOTA chelator comprising a radionuclide.
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