Study of XL647 in Subjects With Non-Small-Cell Lung Cancer

PHASE2CompletedINTERVENTIONAL
Enrollment

55

Participants

Timeline

Start Date

July 31, 2006

Primary Completion Date

May 31, 2010

Study Completion Date

August 31, 2010

Conditions
Non-small-cell Lung Cancer
Interventions
DRUG

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.

Trial Locations (7)

10021

Memorial Sloan Kettering Cancer Center, New York

34952

Hematology Oncology Associates of the Treasure Coast, Port Saint Lucie

44106

Case Western Reserve University, University Hospitals of Cleveland, Cleveland

48201

Wayne University, Wertz Clinical Cancer Center, Karmanos Center, Detroit

60637

University of Chicago, Chicago

61801

Carle Cancer Center, Urbana

02114

Massachusetts General Hospital, Boston

All Listed Sponsors
lead

Kadmon Corporation, LLC

INDUSTRY

NCT00364780 - Study of XL647 in Subjects With Non-Small-Cell Lung Cancer | Biotech Hunter | Biotech Hunter