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Assessment of Safety and Efficacy of Vilaprisan in Subjects With Uterine Fibroids — ASTEROID 7  

Uterine Fibroids Clinical Trial

Official title:
A Randomized, Parallel-group, Double-blind Placebo-controlled, Multicenter Study to Assess the Efficacy and Safety of Vilaprisan in Subjects With Uterine Fibroids

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03699176
Study type Interventional
Source Bayer
Contact
Status Withdrawn
Phase Phase 3
Start date October 27, 2018
Completion date December 25, 2019
View Details
See also
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