6
Participants
Start Date
April 2, 2019
Primary Completion Date
February 28, 2023
Study Completion Date
February 28, 2023
BAY73-4506 (Regorafenib, Stivarga)
Regorafenib is administered orally as 20 or 40 mg tablets at the dose that each patient received during the last cycle of the feeder trial. The dose may be either 60, 80, 120 or 160 mg once daily for 3 weeks of every 4-week cycle (3 weeks on, 1 week off).
Tampa General Medical Group, Tampa
A.O.U. Careggi, Florence
Universitätsklinikum Köln, Cologne
Eberhard-Karls-Universität Tübingen, Tübingen
Saiseikai Utsunomiya Hospital, Utsunomiya
Mount Vernon Hospital, Northwood
Lead Sponsor
Bayer
INDUSTRY