23
Participants
Start Date
January 31, 2014
Primary Completion Date
June 30, 2016
Study Completion Date
September 30, 2016
PG545
PG545 will be administered once weekly, as a one hour IV infusion. Patients will be treated until they exhibit disease progression, withdraw due to poor tolerability, or the study reaches its defined end-point. This study is a dose escalation study with doses of 25 mg to 250 mg anticipated.
Nucleus Network Ltd, Melbourne
Linear Clinical Research Ltd, Nedlands
Zucero Pty Ltd
INDUSTRY