Evaluating the Safety and Efficacy of Proellex® in Premenopausal Women With Symptomatic Uterine Fibroids
A Phase III, Three-Arm, Parallel Design, Placebo-Controlled, Randomized, Double-Blind, Multicenter Study Evaluating the Safety and Efficacy of Proellex® (CDB-4124) in the Treatment of Premenopausal Women With Symptomatic Uterine Fibroids
Sponsor: Repros Therapeutics Inc.
Terminated
Repros stopped the study for safety and FDA put the study on hold for safety.
Other terminated trials from Repros Therapeutics Inc.
- Uterine Fibroids · Phase PHASE2 · May 2017
- Uterine Fibroids · Phase PHASE2 · Aug 2009
- Anemia · Phase PHASE3 · Aug 2009
- Uterine Fibroids · Phase PHASE3 · Aug 2009
- Uterine Fibroids · Phase PHASE3 · Aug 2009
More terminations from Repros Therapeutics Inc.
A PHASE3 clinical study on Uterine Fibroids, this trial is terminated or withdrawn. The trial is conducted by Repros Therapeutics Inc. and has accumulated 7 data snapshots since 2009. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Status Flow
Change History
7 versions recorded-
Sep 2024 — Present [monthly]
Terminated PHASE3
-
Jul 2024 — Sep 2024 [monthly]
Terminated PHASE3
-
Dec 2021 — Jul 2024 [monthly]
Terminated PHASE3
-
Jan 2021 — Dec 2021 [monthly]
Terminated PHASE3
-
Jun 2018 — Jan 2021 [monthly]
Terminated PHASE3
▶ Show 2 earlier versions
-
Feb 2017 — Jun 2018 [monthly]
Terminated PHASE3
-
Jan 2017 — Feb 2017 [monthly]
Terminated PHASE3
First recorded
Feb 2009
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Repros Therapeutics Inc.
For direct contact, visit the study record on ClinicalTrials.gov .