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A Phase 3, Multicentre, Randomized, Double-blind, Placebo-controlled Study Investigating the Efficacy and Safety of Daily Oral Administration of OBE2109 Alone and in Combination With Add-back Therapy for the Management of Heavy Menstrual Bleeding Associated With Uterine Fibroids in Premenopausal Women
Conditions
Interventions
OBE2109
Placebo to match OBE2109
+2 more
Locations
96
United States
Site reference ID 905
Chino, California, United States
Site reference ID 918
Huntington Park, California, United States
Site reference ID 902
San Diego, California, United States
Site reference ID 903
Denver, Colorado, United States
Site reference ID 913
Bradenton, Florida, United States
Site reference ID 912
Orlando, Florida, United States
Start Date
May 23, 2017
Primary Completion Date
September 16, 2019
Completion Date
October 4, 2020
Last Updated
March 5, 2021
NCT05922657
NCT06634719
NCT05862272
NCT07474688
NCT02100904
NCT03948789
Lead Sponsor
ObsEva SA
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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