drugset / Trial / NCT04476329

Optimization for Regorafenib in HCC

NCT04476329

Phase 2 Terminated 7 enrolled SC Liver Research Consortium, LLC Bayer · collab
RandomizedParallel-groupOpen-labelTreatment

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.

Timeline

Start
2021-01-21
Primary completion
2021-10-13
Completion
2021-12-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Regorafenib Small molecule 160 mg Oral