6
Participants
Start Date
September 30, 2009
Primary Completion Date
May 31, 2010
Study Completion Date
May 31, 2010
oral erlotinib and pulsed doses of oral AT-101
Patients will receive oral erlotinib 100 mg daily and pulsed doses of oral AT-101 given 40 mg twice daily on days 1-3 of a 21-day cycle. If the initial combination of erlotinib and AT-101 is tolerated, dose escalation of erlotinib to 150 mg daily will be allowed at the discretion of the treating investigator at the start of cycle 2. Patients will continue receiving treatment on study until they refuse further therapy, develop evidence of progressive disease, or develop unacceptable toxicity or a medical condition that would, in the judgment of the investigator,
Memorial Sloan Kettering Cancer Center, New York
Collaborators (1)
Ascenta Therapeutics
INDUSTRY
Memorial Sloan Kettering Cancer Center
OTHER