Evaluating the Safety and Efficacy of Proellex® in Premenopausal Women With Symptomatic Uterine Fibroids
Public ClinicalTrials.gov record NCT00853567. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
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
Study identification
- NCT ID
- NCT00853567
- Recruitment status
- Terminated
- Study type
- Interventional
- Phase
- Phase 3
- Lead sponsor
- Repros Therapeutics Inc.
- Industry
- Enrollment
- 71 participants
Conditions and interventions
Conditions
Interventions
- Proellex Drug
- placebo Other
Drug · Other
Eligibility (public fields only)
- Age range
- 18 Years to 48 Years
- Sex
- Female
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Jan 31, 2009
- Primary completion
- Jul 31, 2009
- Completion
- Jul 31, 2009
- Last update posted
- Aug 20, 2014
2009
United States locations
- U.S. sites
- 17
- U.S. states
- 8
- U.S. cities
- 13
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Advanced Clinical Research Institute | Anaheim | California | 92801 | — |
| Impact Clinical Trials | Los Angeles | California | 90057 | — |
| National Institute of Clinical Research | Los Angeles | California | 90057 | — |
| Impact Clinical Trials | Los Angeles | California | 90211 | — |
| Segal Institute for Clinical Research | Miami | Florida | 33161 | — |
| Comprehensive Clinical Trials, LLC | West Palm Beach | Florida | 33409 | — |
| Phoenix Women's Center (eCast0 | College Park | Georgia | 30349 | — |
| Clinical Trials Select (eCast) | Decatur | Georgia | 30030 | — |
| Dekalb Gynecology Associates/Legacy Obstetrics & Gynecology (eCast) | Decatur | Georgia | 30035 | — |
| Medical Network for Education and Research | Decatur | Georgia | 30333 | — |
| Smith & Hackney (eCast) | Morrow | Georgia | 30260 | — |
| Bluegrass Clinical Research, Inc. | Louisville | Kentucky | 40291 | — |
| Central Brooklyn Medical Group (eCast) | Brooklyn | New York | 11205 | — |
| Rapid Medical Research, Inc. (Elite) | Cleveland | Ohio | 44122 | — |
| HWC Women's Research Center | Englewood | Ohio | 45322 | — |
| Chattanooga Medical Research, LLC | Chattanooga | Tennessee | 37404 | — |
| Center for Women's Medicine | Houston | Texas | 77079 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT00853567, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Aug 20, 2014 · Synced Jul 21, 2026
Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.
Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00853567 live on ClinicalTrials.gov.