发明名称 Treatment of cancer with elevated dosages of soluble FGFR1 fusion proteins
摘要 The present invention provides methods of treating a patient having a cancer comprising administering to the patient a soluble Fibroblast Growth Factor Receptor 1 (FGFR1) fusion protein such as an extracellular domain of an FGFR1 polypeptide linked to an Fc polypeptide or another fusion partner. The fusion protein may be administered at a dose of at least about 2 mg/kg body weight. In some embodiments, the patient has a fibroblast growth factor-2 (FGF-2) plasma concentration of at least 6 pg/ml. In some embodiments, the cancer is characterized by a Fibroblast Growth Factor Receptor 2 (FGFR2) having a ligand-dependent activating mutation.
申请公布号 US9475871(B2) 申请公布日期 2016.10.25
申请号 US201414551782 申请日期 2014.11.24
申请人 FIVE PRIME THERAPEUTICS, INC. 发明人 Keer Harold
分类号 C07K16/22;C07K14/71 主分类号 C07K16/22
代理机构 McNeill Baur PLLC 代理人 McNeill Baur PLLC
主权项 1. A method of treating a human having a cancer, the method comprising: reducing the fibroblast growth factor-2 (FGF-2) plasma concentration of the human below 4 pg/ml for at least one week by administering to the human a soluble Fibroblast Growth Factor Receptor 1 (FGFR1) fusion protein at a dose of at least about 2 mg/kg body weight, wherein the fusion protein comprises an extracellular domain of an FGFR1 polypeptide linked to a fusion partner, and wherein the human has an FGF-2 plasma concentration of at least 6 pg/ml prior to administration of the soluble FGFR1 fusion protein as determined according to an electrochemiluminescence assay, which utilizes an anti-FGF-2 antibody as the primary antibody and a ruthenium metal chelate anti-human growth factor antibody blend as the secondary antibody.
地址 South San Francisco CA US