49
Participants
Start Date
April 30, 2008
Primary Completion Date
May 31, 2009
Study Completion Date
April 2, 2019
Regorafenib (Stivarga, BAY73-4506)
Patients will be treated with BAY73-4506 160 mg po qd for 3 weeks of every 4 week cycle (i.e., 3 weeks on, 1 week off). Patients will continue treatment with BAY73-4506 until disease progression, intolerable toxicity, or patient refusal to continue with the study or investigator decision to remove the patient from study.
Berlin
Hamburg
Nantes
Frankfurt am Main
Paris
Houston
Los Angeles
Helsinki
Turku
Dresden
Bialystok
Lublin
Poznan
Leicester
Bristol
Cambridge
London
Northwood
Lead Sponsor
Bayer
INDUSTRY