drugset / Trial / NCT03699176

Assessment of Safety and Efficacy of Vilaprisan in Subjects With Uterine Fibroids

NCT03699176

Phase 3 Withdrawn Bayer
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study is to show superiority of vilaprisan in the treatment of heavy menstrual bleeding (HMB) in subjects with uterine fibroids compared to placebo.The secondary objectives of this study are to additionally evaluate the efficacy and safety of vilaprisan in subjects with uterine fibroids.

Timeline

Start
2018-10-27
Primary completion
2019-12-25
Completion
2019-12-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Vilaprisan Other / unclassified 2 mg Oral

Indications