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Study Evaluating the Safety and Efficacy of Proellex® in the Treatment of Endometriosis-extension Study

Endometriosis Clinical Trial

Official title:
A Randomized, Double-blind Study Evaluating the Safety and Efficacy of Proellex® in the Treatment of Premenopausal Women With Symptomatic Endometriosis-extension Study

Clinical Trial Summary

ZPE-201 Extension of treatment

Clinical Trial Description

This is an extension of the phase II, three-arm, parallel design, dose-ranging, placebo-controlled, randomized, double-blind, multicenter study in which placebo or one (1) of two (2) dose levels of Proellex® was administered once-daily for four (4) months. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00958412
Study type Interventional
Source Repros Therapeutics Inc.
Contact
Status Terminated
Phase Phase 2
Start date February 28, 2009
Completion date August 31, 2009
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