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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Elagolix | Small molecule | 300 mg | — |
| Subject | Estradiol | Other / unclassified | 1 mg | — |
| Subject | Norethindrone | Unknown | 0.5 mg | — |