Viewing Study NCT01069120

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Ignite Creation Date: 2025-12-25 @ 4:14 AM

Ignite Modification Date: 2026-01-08 @ 9:00 AM

Study NCT ID: NCT01069120

Status: TERMINATED

Last Update Posted: 2014-08-21

First Post: 2010-02-10

Is Gene Therapy: True

Has Adverse Events: True

Brief Title: Safety of 25 and 50 mg Proellex® in the Treatment of 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