A Phase II Study of GSK1363089 (Formerly XL880) for Papillary Renal-Cell Carcinoma (PRC)



Status:Completed
Conditions:Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:12/13/2017
Start Date:June 30, 2006
End Date:August 18, 2010

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A Phase II Study of the c-MET RTK Inhibitor XL880 in Subjects With Papillary Renal-Cell Carcinoma

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.


Inclusion Criteria:

- Histologically confirmed diagnosis of PRC with metastatic disease or bilateral
multifocal renal tumors localized to kidneys. Measurable disease, ECOG performance
status of
- 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
We found this trial at
12
sites
Indianapolis, Indiana 46202
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Indianapolis, IN
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Bethesda, Maryland 20892
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Bethesda, MD
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Boston, Massachusetts 02115
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Boston, MA
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Cleveland, Ohio 44195
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Cleveland, OH
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Detroit, Michigan 48202
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Detroit, MI
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Greenbrae, California 94904
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Greenbrae, CA
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Nashville, Tennessee 37203
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Nashville, TN
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New Brunswick, New Jersey 08901
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New Brunswick, NJ
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Philadelphia, Pennsylvania 19104
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Philadelphia, PA
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San Antonio, Texas 78258
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San Antonio, TX
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San Francisco, California 94115
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San Francisco, CA
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Stanford, California 94305
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Stanford, CA
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