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Clinical trial

A Phase III, Three-arm, Parallel Design, Placebo-controlled, Randomized, Double-blind, Multicenter Study Evaluating the Safety and Efficacy of Proellex® (CDB-4124) in the Treatment of Premenopausal Women With Symptomatic Uterine Fibroids

NCT00735553 is registered in ClinicalTrials.gov with Repros Therapeutics Inc. as lead sponsor.

NCT NCT00735553
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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase III, Three-arm, Parallel Design, Placebo-controlled, Randomized, Double-blind, Multicenter Study Evaluating the Safety and Efficacy of Proellex® (CDB-4124) in the Treatment of Premenopausal Women With Symptomatic Uterine Fibroids
Lead sponsor
Repros Therapeutics Inc.
Phase
Phase 3
Overall status
Terminated
Start date
August 31, 2008
Completion date
August 31, 2009
Enrollment
77 (actual)
Sites
15

Conditions

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

uterine fibroids