25
Participants
Start Date
January 31, 2013
Primary Completion Date
March 31, 2015
Study Completion Date
March 31, 2015
G-202
G-202 administered by intravenous infusion (IV, in the vein) on Days 1, 2 and 3 of each 28-day cycle until progression or development of unacceptable toxicity
Mary Crowley Cancer Research Center, Dallas
Oncology Consultants, PA, Houston
University of Texas Health Sciences Center at Houston, Memorial Hermann Cancer Center, Houston
The University of Texas Health Science Center at San Antonio, San Antonio
Lead Sponsor
GenSpera, Inc.
INDUSTRY