Viewing Study NCT01069120


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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:

Organization Data

Organization:
Class: INDUSTRY
Study ID: ZPU-307
Study Type: None
Study Domain: None
Study Link: None
Lead Sponsor:
Lead Sponsor Class: INDUSTRY
Responsible Party:
Responsible Party Title:
Responsible Party Type: SPONSOR
Responsible Party Affiliation:
Old Name: None
Old Organization: None

Collaborators