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 |