Kidney Cancer Clinical Trial
A Phase II Study of GSK1363089 (Formerly XL880) for Papillary Renal-Cell Carcinoma (PRC)
Summary
This clinical study is being conducted at multiple sites to determine the best confirmed response rate, safety, and tolerability of GSK1363089 treatment in papillary renal cell carcinoma. Papillary renal cell carcinoma may be classified into hereditary and sporadic forms; subjects with either classification will be accepted into this study.
Eligibility Criteria
Inclusion Criteria:
Histologically confirmed diagnosis of PRC with metastatic disease or bilateral multifocal renal tumors localized to kidneys. Measurable disease, ECOG performance status of = 2.
Adequate bone marrow reserve, hepatic, renal, and cardiovascular function.
Exclusion Criteria:
Radiation to >/=25% of bone marrow within 14 days of GSK1363089, more than 1 prior anti-cancer therapy, received prior treatment with a c-met inhibitor, brain metastases,
Any uncontrolled intercurrent illness,
Pregnant or breastfeeding,
HIV positive
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There are 12 Locations for this study
Greenbrae California, 94904, United States
San Francisco California, 94115, United States
Stanford California, 94305, United States
Indianapolis Indiana, 46202, United States
Bethesda Maryland, 20892, United States
Boston Massachusetts, 02115, United States
Detroit Michigan, 48201, United States
New Brunswick New Jersey, 08901, United States
Cleveland Ohio, 44195, United States
Philadelphia Pennsylvania, 19104, United States
Nashville Tennessee, 37232, United States
San Antonio Texas, 78229, United States
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