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

Outcome

Met primary endpoint

registry Relugolix Plus E2/NETA (Group A) vs Placebo (Group C); p <0.0001; Treatment Difference 56.47 (95% CI 46.45 to 66.49) NCT03103087 ↗

release “LIBERTY 1 and LIBERTY 2 each met the primary endpoint, with 73.4% and 71.2% of women in the relugolix combination therapy groups achieving the responder criteria” pfizer.com ↗

release “LIBERTY 1 and 2 met their primary endpoints (p < 0.0001)” pfizer.com ↗

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