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Clinical trial

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

NCT00958412 is registered in ClinicalTrials.gov with Repros Therapeutics Inc. as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Randomized, Double-blind Study Evaluating the Safety and Efficacy of Proellex® in the Treatment of Premenopausal Women With Symptomatic Endometriosis-extension Study
Lead sponsor
Repros Therapeutics Inc.
Phase
Phase 2
Overall status
Terminated
Start date
February 28, 2009
Completion date
August 31, 2009
Enrollment
18 (actual)
Sites
8

Conditions

As the registry lists them; a condition with its own page is linked.