Last updated on August 2018

A Phase 3, multicenter, randomized, double-blind, placebo-controlled study investigating the efficacy and safety of daily oral administration of OBE2109 alone and in combination with add-back therapy for the management of heavy menstrual bleeding associated with uterine fibroids in premenopausal women.


Brief description of study

A phase 3 study of OBE2109 in subjects with heavy menstrual bleeding associated with uterine fibroids.

Clinical Study Identifier: TX201695

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IACT Health

Located in: Columbus, GA USA
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Recruitment Status: Open


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