The purpose of this research study is to determine the highest dose of the drug (BMS-690514) that can be safely given to patients with advanced cancer.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
89
Tablets, Oral, up to 300 mg, once daily, up to 24 mos
Indiana University Med Center
Indianapolis, Indiana, United States
The University Of Texas Md Anderson Cancer Center
Houston, Texas, United States
Local Institution
Ottawa, Ontario, Canada
Local Institution
Toronto, Ontario, Canada
Safety
Time frame: results of weekly vital sign measurements, ECGs, laboratory tests and physical exams, echocardiograms every 8 weeks
Highest dose tolerated
Time frame: continuous medical review of adverse event reports
Effective dose or doses of BMS-690514
Time frame: tumor measurement by imaging every eight weeks. Continuous medical review of adverse event reports
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Local Institution
Toulouse, France
Local Institution
Villejuif, France
Local Institution
Barcelona, Spain