1
Participants
Start Date
April 30, 2008
Primary Completion Date
October 31, 2008
Study Completion Date
October 31, 2008
KOS-1584
25 mg/m2, IV (in the vein) on day 1 and 8 of each 21 day cycle until progression or unacceptable toxicity develops.
Consultants In Blood Disorders & Cancer, Louisville
Lead Sponsor
Bristol-Myers Squibb
INDUSTRY