drugset / Trial / NCT03271489

Long-Term Safety Study of Elagolix in Combination With Estradiol/Norethindrone Acetate for the Management of Heavy Menstrual Bleeding Associated With Uterine Fibroids in Premenopausal Women

NCT03271489

Phase 3 Completed 478 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This randomized multicenter phase 3b study seeks to evaluate the safety of elagolix in combination with estradiol/norethindrone acetate for the management of heavy menstrual bleeding associated with uterine fibroids in premenopausal women. This study was double-blind (DB) during the first 12 months and open-label (OL) for the next 36 months.

Timeline

Start
2017-09-13
Primary completion
2024-06-28
Completion
2024-06-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Elagolix Small molecule 300 mg
Subject Estradiol Other / unclassified 1 mg
Subject Norethindrone Unknown 0.5 mg

Indications