| CPC C07K 16/3084 (2013.01) [A61K 31/437 (2013.01); A61K 31/53 (2013.01); A61K 38/193 (2013.01); A61P 35/00 (2018.01); A61K 2039/505 (2013.01)] | 15 Claims |
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1. A method of treating a human subject having chemoresistant neuroblastoma, comprising administering to the subject a therapeutically effective amount of an anti-GD2 antibody or an antigen-binding fragment thereof, and at least one hematopoietic growth factor, irinotecan, and temozolomide,
wherein the anti-GD2 antibody or antigen-binding fragment thereof each comprises:
a) a heavy chain variable region comprising a CDR1 comprising amino acid residues 31 to of SEQ ID NO: 4, a CDR2 comprising amino acid residues 50 to 65 of SEQ ID NO: 4, and a CDR3 comprising amino acid residues 98 to 108 of SEQ ID NO: 4, and a light chain variable region comprising a CDR1 comprising amino acid residues 24 to 34 of SEQ ID NO: 5, a CDR2 comprising amino acid residues 50 to 56 of SEQ ID NO: 5, and a CDR3 comprising amino acid residues 89 to 94 of SEQ ID NO: 5; or
b) a heavy chain variable region comprising a CDR1 comprising amino acid residues 31 to of SEQ ID NO: 11, a CDR2 comprising amino acid residues 50 to 65 of SEQ ID NO: 11, and a CDR3 comprising amino acid residues 98 to 108 of SEQ ID NO: 11, and a light chain variable region comprising a CDR1 comprising amino acid residues 24 to 34 of SEQ ID NO: 5, a CDR2 comprising amino acid residues 50 to 56 of SEQ ID NO: 5, and a CDR3 comprising amino acid residues 89 to 94 of SEQ ID NO: 5.
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