Clinical Trials Directory

Trials / Completed

CompletedNCT02147158

A Study of the Efficacy and Safety of Ulipristal Acetate Intermittent Treatment for Abnormal Uterine Bleeding Associated With Leiomyomas

A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Intermittent Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
432 (actual)
Sponsor
Allergan · Industry
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Not accepted

Summary

This study will evaluate the superiority of ulipristal acetate versus placebo for the treatment of abnormal uterine bleeding associated with uterine fibroids

Conditions

Interventions

TypeNameDescription
DRUGUlipristal acetate (UPA)Ulipristal acetate (UPA) tablet.
DRUGPlaceboMatching placebo tablet.

Timeline

Start date
2014-01-29
Primary completion
2016-11-24
Completion
2016-11-24
First posted
2014-05-26
Last updated
2019-06-04
Results posted
2019-06-04

Locations

63 sites across 2 countries: United States, Canada

Regulatory

Source: ClinicalTrials.gov record NCT02147158. Inclusion in this directory is not an endorsement.

A Study of the Efficacy and Safety of Ulipristal Acetate Intermittent Treatment for Abnormal Uterine Bleeding Associated (NCT02147158) · Clinical Trials Directory