Viewing Study NCT00702702

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Ignite Modification Date: 2025-12-26 @ 2:32 AM

Study NCT ID: NCT00702702

Status: TERMINATED

Last Update Posted: 2014-08-21

First Post: 2008-06-18

Is NOT Gene Therapy: False

Has Adverse Events: True

Brief Title: Safety and Efficacy of Proellex in Pre-menopausal Anemic Women With Symptomatic Uterine Fibroids

Sponsor: Repros Therapeutics Inc.

Organization:

Overview Dates Organization Conditions Design Enrollment Locations Outcomes Modules Raw JSON

Study Modules

Identification Module Status Module Sponsor Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms Interventions Module Outcomes Module Eligibility Module Contacts Locations Module Adverse Events Module Baseline Characteristics Module Participant Flow Module