drugset / Trial / NCT03103087

LIBERTY 2: Efficacy & Safety Study of Relugolix in Women With Heavy Menstrual Bleeding Associated With Uterine Fibroids

NCT03103087

Phase 3 Completed 382 enrolled Myovant Sciences GmbH
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to determine the benefit of relugolix 40 milligrams (mg) once a day co-administered with estradiol (E2) 1 mg and norethindrone acetate (NETA) 0.5 mg compared with placebo for 24 weeks on heavy menstrual bleeding associated with uterine fibroids.

Timeline

Start
2017-06-14
Primary completion
2019-07-10
Completion
2020-09-16

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Estradiol/norethindrone acetate Unknown 0.5 mg Oral
Subject Estradiol/norethindrone acetate Unknown 1 mg Oral
Subject Relugolix Small molecule 40 mg Oral

Indications