A randomized, double-blind, placebo-controlled phase III study of regorafenib plus BSC versus placebo plus BSC in patients with metastatic colorectal cancer (CRC) who have progressed after standard therapy

Registry ID
EUCTR2009-012787-14
Source registry
EUCTR
Status
Completed
Phase
PHASE3
Sponsor
Bayer HealthCare AG
Start date
2010-07-26
Last update
2026-08-16

Conditions

Summary

To evaluate efficacy and safety of regorafenib in patients with metastatic colorectal cancer (CRC) who have progressed after standard therapies. The primary efficacy endpoint of this study is Overall survival

Locations

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