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Assess Safety and Efficacy of Vilaprisan in Subjects With Uterine Fibroids (ASTEROID 4)
The primary objective of this study was 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 were to additionally evaluate the efficacy and safety of vilaprisan in subjects with uterine fibroids
Details
| Lead sponsor | Bayer |
|---|---|
| Phase | PHASE3 |
| Status | TERMINATED |
| Enrolment | 103 |
| Start date | Wed Jan 24 2018 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Wed Jun 30 2021 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Uterine Fibroids
Interventions
- Vilaprisan (BAY1002670)
- Placebo
Countries
Japan, Russia, Ukraine, United States, Czechia