FIELD: biotechnology.
SUBSTANCE: method of treating a malignant neoplasm in a mammal is described, comprising administering an effective amount of a liquid pharmaceutical composition of an anti-human PD-1 antibody. This method comprises 25-100 mg/ml of anti-human PD-1 antibody; about 70 mg/ml of sucrose; approximately 0.2 mg/ml of polysorbate 80; and approximately 10 mM of histidine buffer at pH of 5.0-6.0, where the human anti-PD-1 antibody comprises: a light chain comprising three CDR sequences of SEQ ID NO: 15.016 and 17; and a heavy chain comprising three CDR sequences of SEQ ID NOs: 18, 19 and 20. In one embodiment, the human anti-PD-1 antibody comprises: a light chain comprising amino acid residues of 20-237 of SEQ ID NO: 36 and a heavy chain comprising amino acid residues of 20-466 of SEQ ID NO: 31.
EFFECT: invention extends the arsenal by treating malignant neoplasms in mammals using an anti-human PD-1 antibody.
5 cl, 18 dwg, 3 ex, 6 tbl
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Authors
Dates
2017-10-12—Published
2012-03-29—Filed