CompletedPhase 3NCT02147158
A Study of the Efficacy and Safety of Ulipristal Acetate Intermittent Treatment for Abnormal Uterine Bleeding Associated With Leiomyomas
Studying Muscular tumor
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Allergan
- Principal Investigator
- Anna ChanAllergan
- Intervention
- Ulipristal acetate (UPA)(drug)
- Enrollment
- 432 target
- Eligibility
- 18-50 years · FEMALE
- Timeline
- 2014 – 2016
Study locations (30)
- Watson Investigational Site 138, Mesa, Arizona, United States
- Watson Investigational Site 147, Phoenix, Arizona, United States
- Watson Investigational Site 106, Scottsdale, Arizona, United States
- Watson Investigational Site 124, Tucson, Arizona, United States
- Watson Investigational Site 155, Little Rock, Arkansas, United States
- Watson Investigational Site 155, Encino, California, United States
- Watson Investigational Site 157, Hawaiian Gardens, California, United States
- Watson Investigational Site 134, La Mesa, California, United States
- Watson Investigational Site 127, San Diego, California, United States
- Watson Investigational Site 151, San Diego, California, United States
- Watson Investigational Site 159, Denver, Colorado, United States
- Watson Investigational Site 131, Clearwater, Florida, United States
- Watson Investigational Site 135, Miramar, Florida, United States
- Watson Investigational Site 132, North Miami, Florida, United States
- Watson Investigational Site 161, Orlando, Florida, United States
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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