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

Status: Completed

Phase of Trial: Phase II

Latest Information Update: 14 Jan 2020

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At a glance

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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