An Extension Study of 12 mg Proellex® (Telapristone Acetate) Administered Orally in the Treatment of Premenopausal Women With Confirmed Symptomatic Uterine Fibroids
An Open-Label Extension Study of 12 mg Proellex® (Telapristone Acetate) Administered Orally in the Treatment of Premenopausal Women With Confirmed Symptomatic Uterine Fibroids
Sponsor: Repros Therapeutics Inc.
Terminated
Business decision
Other terminated trials from Repros Therapeutics Inc.
- Uterine Fibroids · Phase PHASE2 · Aug 2009
- Anemia · Phase PHASE3 · Aug 2009
- Uterine Fibroids · Phase PHASE3 · Aug 2009
- Uterine Fibroids · Phase PHASE3 · Aug 2009
- Anemia · Phase PHASE3 · Aug 2009
More terminations from Repros Therapeutics Inc.
This PHASE2 trial investigates Uterine Fibroids and is currently terminated or withdrawn. Repros Therapeutics Inc. leads this study, which shows 9 recorded versions since 2016 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.
Status Flow
Change History
9 versions recorded-
Sep 2024 — Present [monthly]
Terminated PHASE2
-
Jul 2024 — Sep 2024 [monthly]
Terminated PHASE2
-
Jan 2021 — Jul 2024 [monthly]
Terminated PHASE2
-
Jul 2019 — Jan 2021 [monthly]
Terminated PHASE2
-
Jul 2018 — Jul 2019 [monthly]
Terminated PHASE2
▶ Show 4 earlier versions
-
Jun 2018 — Jul 2018 [monthly]
Terminated PHASE2
-
Aug 2017 — Jun 2018 [monthly]
Terminated PHASE2
Status: Active Not Recruiting → Terminated
-
Feb 2017 — Aug 2017 [monthly]
Active Not Recruiting PHASE2
-
Jan 2017 — Feb 2017 [monthly]
Active Not Recruiting PHASE2
First recorded
Jul 2016
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 .