23
Participants
Start Date
January 31, 2011
Primary Completion Date
May 31, 2013
Study Completion Date
May 31, 2013
GO-203-2c
GO-203-2c Injection is a non-preserved, sterile, ready-to-use liquid dosage form provided in a glass vial with rubber closure and crimp seal. Injection will be added to the contents of an intravenous bag (of 0.9% NS, D5W or sterile water) to a final concentration of between 0.03 - 0.3 mg/ml (preferable in 100 mls or greater) and administered as a single agent intravenously over 60 minutes. A treatment cycle will consist of a daily IV dose administered for 21 consecutive days followed by a 7 day rest.
University of Texas Health Science Center San Antonio, San Antonio
TGen Clinical Research Service, Scottsdale
Cedars-Sinai Medical Center, Los Angeles
Beth Israel Deaconess Medical Center, Boston
Lead Sponsor
Genus Oncology, LLC
INDUSTRY