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A Safety and Pharmacokinetic Study of 100 mg, 150 mg and 200 mg of Proellex® Taken for Seven Days by Healthy Adult Female Subjects

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Trial Profile

A Safety and Pharmacokinetic Study of 100 mg, 150 mg and 200 mg of Proellex® Taken for Seven Days by Healthy Adult Female Subjects

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 01 Oct 2014

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At a glance

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

    • Most Recent Events

    • 11 Feb 2010 Actual number of patients (18) added as reported by ClinicalTrials.gov.
    • 31 Oct 2008 Added October 2008 as the actual completion date, based on information from ClinicalTrials.gov.
    • 13 May 2008 Status changed from recruiting to completed, as reported by Repros Therapeutics.

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