Overview

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

Status:
Completed
Trial end date:
2020-09-16
Target enrollment:
Participant gender:
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.
Phase:
Phase 3
Details
Lead Sponsor:
Myovant Sciences GmbH
Treatments:
Estradiol
Estradiol 17 beta-cypionate
Estradiol 3-benzoate
Norethindrone
Norethindrone Acetate
Polyestradiol phosphate
Relugolix