发明名称 |
Methods and monitoring of treatment with a Wnt pathway inhibitor |
摘要 |
Methods for treating diseases such as cancer comprising administering a Wnt pathway inhibitor, either alone or in combination with other anti-cancer agents, and monitoring for skeletal-related side effects and/or toxicity. |
申请公布号 |
US9359444(B2) |
申请公布日期 |
2016.06.07 |
申请号 |
US201414171151 |
申请日期 |
2014.02.03 |
申请人 |
OncoMed Pharmaceuticals Inc. |
发明人 |
Dupont Jakob;Stagg Robert J. |
分类号 |
A61K39/395;A61K38/17;C07K16/28;C07K16/30;A61K31/675;A61K45/06;G01N33/574;A61K39/00 |
主分类号 |
A61K39/395 |
代理机构 |
Sterne, Kessler, Goldstein & Fox P.L.L.C. |
代理人 |
Sterne, Kessler, Goldstein & Fox P.L.L.C. |
主权项 |
1. A method for reducing a skeletal-related side effect and/or toxicity in a human subject having cancer and receiving treatment with a Wnt pathway inhibitor for the cancer, comprising:
(a) administering a therapeutically effective amount of a Wnt pathway inhibitor to the subject; (b) determining the level of collagen type 1 cross-linked C-telopeptide (β-CTX) in a sample from the subject after the administration of the Wnt pathway inhibitor; and (c) administering to the subject a therapeutically effective amount of a bisphosphonate if the level of β-CTX in the sample is higher than a predetermined level of the β-CTX; and wherein the Wnt pathway inhibitor is: (i) an antibody that specifically binds human FZD1, FZD2, FZD5, FZD7, and FZD8 and comprises a heavy chain CDR1 comprising GFTFSHYTLS (SEQ ID NO:1), a heavy chain CDR2 comprising VISGDGSYTYYADSVKG (SEQ ID NO:2), and a heavy chain CDR3 comprising NFIKYVFAN (SEQ ID NO:3), and a light chain CDR1 comprising SGDNIGSFYVH (SEQ ID NO:4), a light chain CDR2 comprising DKSNRPSG (SEQ ID NO:5), and a light chain CDR3 comprising QSYANTLSL (SEQ ID NO:6); or (ii) a soluble receptor comprising a Fri domain of human FZD8 and a human Fc region. |
地址 |
Redwood City CA US |