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Terminated Phase 3 Interventional Results available

Multicenter Study Evaluating the Safety of Proellex® in Premenopausal Women With Uterine Fibroids

ClinicalTrials.gov ID: NCT00737282

Public ClinicalTrials.gov record NCT00737282. 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.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 6:05 PM EDT

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, 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

Study identification

NCT ID
NCT00737282
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Repros Therapeutics Inc.
Industry
Enrollment
175 participants

Conditions and interventions

Interventions

  • Proellex 25 mg Drug
  • Proellex 50 mg Drug

Drug

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
Sep 30, 2008
Primary completion
Jul 31, 2009
Completion
Jul 31, 2009
Last update posted
Aug 20, 2014

2008 – 2009

United States locations

U.S. sites
25
U.S. states
15
U.S. cities
20
Facility City State ZIP Site status
Lynn Institute of the Ozarks Little Rock Arkansas 72205
AWC Clinical Trials LLC Little Rock Arkansas 72223
Impact Clinical Trials Beverly Hills California 80211
Genesis Center for Clinical Research San Diego California 92103
Physician Care Clinical Research, LLC Sarasota Florida 34329
Atlanta Women's Research Inst Atlanta Georgia 30342
Medical Network for Education and Research Decatur Georgia 30033
Soapstone Center for Clinical Research Decatur Georgia 30034
York Clinical Consulting Marrero Louisiana 70072
NECCR Falls River LLC Fall River Massachusetts 02720
ClinSite, LLC Ann Arbor Michigan 48106
Female Pelvic Medicine Grand Rapids Michigan 49503
Alegent Research Omaha Nebraska 68124
Hawthorne Medical Research, Inc. Winston-Salem North Carolina 27103
Lyndhurst Gynecologic Associates Winston-Salem North Carolina 27103
Clinical Trials of America Eugene Oregon 97408
Thomas Jefferson University - Jefferson Center for Women's Medical Specialties Philadelphia Pennsylvania 19107-5127
University Medical Group, Dept of OB/GYN Greenville South Carolina 29605
Greenville Pharmaceutical Research Greenville South Carolina 29615
Memphis Women's Healthcare Memphis Tennessee 38119
Women's Care Center, PLC Research Memphis Associates Memphis Tennessee 38119
Meharry Medical College Nashville Tennessee 37208
Women Partners in Health Austin Texas 78705
Willowbend Health & Wellness Associates Plano Texas 75093
Medical Associates Inc. Menomonee Falls Wisconsin 53051

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 NCT00737282, 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

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00737282 live on ClinicalTrials.gov.

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