A Clinical Study of Regorafenib in Participants Who Have Been Treated in Previous Bayer-sponsored Regorafenib Studies That Have Been Completed

PHASE2CompletedINTERVENTIONAL
Enrollment

6

Participants

Timeline

Start Date

April 2, 2019

Primary Completion Date

February 28, 2023

Study Completion Date

February 28, 2023

Conditions
Solid Cancer
Interventions
DRUG

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).

Trial Locations (6)

33606

Tampa General Medical Group, Tampa

50134

A.O.U. Careggi, Florence

50937

Universitätsklinikum Köln, Cologne

72076

Eberhard-Karls-Universität Tübingen, Tübingen

321-0974

Saiseikai Utsunomiya Hospital, Utsunomiya

HA6 2RN

Mount Vernon Hospital, Northwood

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY