drugset / Trial / NCT03204318

SPIRIT 1: Efficacy and Safety Study of Relugolix in Women With Endometriosis-Associated Pain

NCT03204318

Phase 3 Completed 638 enrolled Myovant Sciences GmbH
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to determine the benefit and safety of relugolix 40 milligrams (mg) once daily, co-administered with low-dose estradiol (E2) and norethindrone acetate (NETA) compared with placebo for 24 weeks, on dysmenorrhea and on nonmenstrual pelvic pain.

Timeline

Start
2017-12-07
Primary completion
2020-06-09
Completion
2021-04-08

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