Overview

Optimization for Regorafenib in HCC

Status:
Active, not recruiting
Trial end date:
2022-02-28
Target enrollment:
Participant gender:
Summary
This is a randomized, two arm, phase II study of 1st Cycle dose optimization for regorafenib treatment compared to standard dose of regorafenib treatment in HCC patients for whom the physician is intending to treat with regorafenib and who failed any 1st line systemic treatment.
Phase:
Phase 2
Details
Lead Sponsor:
SC Liver Research Consortium, LLC
Collaborator:
Bayer