drugset / Trial / NCT03070951

Efficacy and Safety of OBE2109 in Subjects With Heavy Menstrual Bleeding Associated With Uterine Fibroids

NCT03070951

Phase 3 Completed 511 enrolled ObsEva SA
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study is to demonstrate the superior efficacy versus placebo of OBE2109 alone and in combination with add-back therapy for the reduction of heavy menstrual bleeding associated with uterine fibroids in premenopausal women.

Timeline

Start
2017-05-23
Primary completion
2019-09-16
Completion
2020-10-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Add-back Unknown 1 mg Oral
Subject NETA Unknown 0.5 mg Oral
Subject linzagolix Unknown 100 mg Oral
Subject linzagolix Unknown 200 mg Oral