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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.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
GSK Investigational Site
Greenbrae, California, United States
GSK Investigational Site
San Francisco, California, United States
GSK Investigational Site
Stanford, California, United States
GSK Investigational Site
Indianapolis, Indiana, United States
GSK Investigational Site
Bethesda, Maryland, United States
GSK Investigational Site
Boston, Massachusetts, United States
GSK Investigational Site
Detroit, Michigan, United States
GSK Investigational Site
New Brunswick, New Jersey, United States
GSK Investigational Site
Cleveland, Ohio, United States
GSK Investigational Site
Philadelphia, Pennsylvania, United States
Start Date
June 30, 2006
Primary Completion Date
August 18, 2010
Completion Date
August 18, 2010
Last Updated
December 11, 2017
74
ACTUAL participants
foretinib (formerly GSK1363089 or XL880)
DRUG
Lead Sponsor
GlaxoSmithKline
NCT07227415
NCT05127824
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05865730