A Phase 2, Multi-Center, Three-Arm, Parallel Design, Randomized, Double-Blind Study to Evaluate the Safety and Efficacy of 6 and 12 mg Proellex (Telapristone Acetate) Administered Orally in the Treatment of Premenopausal Women With Confirmed Symptomatic Endometriosis

Trial Profile

A Phase 2, Multi-Center, Three-Arm, Parallel Design, Randomized, Double-Blind Study to Evaluate the Safety and Efficacy of 6 and 12 mg Proellex (Telapristone Acetate) Administered Orally in the Treatment of Premenopausal Women With Confirmed Symptomatic Endometriosis

Completed
Phase of Trial: Phase II

Latest Information Update: 28 Jul 2017

At a glance

  • Drugs Telapristone (Primary)
  • Indications Endometriosis
  • Focus Therapeutic Use
  • Sponsors Repros Therapeutics
  • Most Recent Events

    • 25 Jul 2017 Status changed from active, no longer recruiting to completed.
    • 07 Sep 2016 Based on the results from this trial the company is preparing to interact with the FDA, according to a Repros Therapeutics media release.
    • 07 Sep 2016 Primary endpoint has been met. (Change in individual BBSS pain scores), according to a Repros Therapeutics media release.
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