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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.

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Trial Profile

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.

Status: Discontinued
Phase of Trial: Phase III

Latest Information Update: 10 Nov 2021

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At a glance

  • Drugs Telapristone (Primary)
  • Indications Uterine leiomyoma
  • Focus Adverse reactions
  • Sponsors Repros Therapeutics

    • Most Recent Events

    • 17 Feb 2010 Actual end date (Aug 2009) and actual number of patients (175) added as reported by ClinicalTrials.gov.
    • 14 Aug 2009 Status changed from suspended to discontinued as reported by ClinicalTrials.gov.
    • 03 Aug 2009 Status changed from recruiting to suspended, according to a Repros Therapeutics media release.

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