55
Participants
Start Date
July 31, 2006
Primary Completion Date
May 31, 2010
Study Completion Date
August 31, 2010
XL647
XL647 will be administered orally as a single agent. XL647 will be supplied as 50 mg tablets. Subjects in the Intermittent 5 \& 9 cohort will receive XL647 at a dose of 350 mg on a 5 days on and 9 days off cycle every 2 weeks for 8 weeks. Subjects in the Daily Dosing cohort will receive XL647 administered daily as a single oral dose of 300 mg. In the absence of progressive disease (PD) and unacceptable XL647-related toxicity, subjects may continue to receive XL647 treatment on their assigned dosing schedule for up to 1 year on this study. Subjects who reach 1 year of treatment with no evidence of disease progression may, with the concurrence of the investigator and the sponsor, continue to receive therapy.
Memorial Sloan Kettering Cancer Center, New York
Hematology Oncology Associates of the Treasure Coast, Port Saint Lucie
Case Western Reserve University, University Hospitals of Cleveland, Cleveland
Wayne University, Wertz Clinical Cancer Center, Karmanos Center, Detroit
University of Chicago, Chicago
Carle Cancer Center, Urbana
Massachusetts General Hospital, Boston
Kadmon Corporation, LLC
INDUSTRY