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A Phase II, Multicenter, Randomized, Placebo-controlled, Double-blinded Study of the Selective Progesterone Receptor Modulator Proellex (CDB-4124) in Pre-menopausal Women With Symptomatic Leiomyomata

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Trial Profile

A Phase II, Multicenter, Randomized, Placebo-controlled, Double-blinded Study of the Selective Progesterone Receptor Modulator Proellex (CDB-4124) in Pre-menopausal Women With Symptomatic Leiomyomata

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 05 Sep 2014

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At a glance

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

    • Most Recent Events

    • 14 Apr 2009 New source identified and integrated (ClinicalTrials.gor record NCT00882258).
    • 01 Apr 2007 Status changed from in progress to completed.
    • 20 Jun 2006 New trial record.

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