drugset / Trial / NCT04756037

Study of the Safety and Contraceptive Efficacy of Relugolix Combination Therapy in Women With Uterine Fibroids or Endometriosis Who Are at Risk for Pregnancy

NCT04756037

Phase 3 Completed 1164 enrolled Sumitomo Pharma Switzerland GmbH
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the contraceptive efficacy of relugolix combination therapy.

Timeline

Start
2021-03-18
Primary completion
2025-02-25
Completion
2026-03-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Estradiol Other / unclassified 1 mg Oral
Subject Norethindrone Unknown 0.5 mg Oral
Subject Relugolix Small molecule 40 mg Oral

Indications

No indication recorded.