Multicenter Study Evaluating the Safety of Proellex® in Premenopausal Women With Uterine Fibroids
A Phase III, Open-Label, Parallel, Randomized, Multicenter Study Evaluating the Safety of 25 And 50 mg Proellex® (CDB-4124) in the Treatment of Premenopausal Women With Symptomatic Uterine Fibroids
Sponsor: Repros Therapeutics Inc.
Terminated
Repros stopped study for safety and FDA put study on hold.
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
- Anemia · Phase PHASE3 · Aug 2009
More terminations from Repros Therapeutics Inc.
Listed as NCT00737282, this PHASE3 trial focuses on Uterine Fibroids and remains terminated or withdrawn. Sponsored by Repros Therapeutics Inc., it has been updated 7 times since 2008, reflecting limited change activity. This study adds to the evidence base for this therapeutic area through structured, versioned documentation.
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
Oct 2008
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 .