drugset / Trial / NCT02584465

REGorafenib vsTamoxifen in Patients With Platinum-sensitive OVARian Carcinoma and Isolated Biological Progression

NCT02584465

Phase 2 Completed 68 enrolled ARCAGY/ GINECO GROUP Bayer · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The objective of this randomized phase II is to evaluate the benefit of regorafenib for ovarian patients who reported a confirmed elevated CA-125 level under surveillance or bevacizumab, compared with tamoxifen.

Timeline

Start
2015-08-28
Primary completion
2021-09-19
Completion
2021-09-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Regorafenib Small molecule 120 mg Oral
Comparator Tamoxifen Small molecule 40 mg

Indications