60
Participants
Start Date
January 31, 2011
Primary Completion Date
August 31, 2015
Study Completion Date
August 31, 2015
PM060184
PM060184 administered intravenously (i.v.) over 10 minutes at a starting dose of 4 mg/m2/day on three consecutive days q2w (on Days 1-3 and 15-17) every 28 days.
START- South Texas Accelerated Research Therapeutics, LLC, San Antonio
Lead Sponsor
PharmaMar
INDUSTRY