drugset / Trial / NCT00437658

Elagolix Versus Subcutaneous Depot Medroxyprogesterone Acetate for the Treatment of Endometriosis

NCT00437658

Phase 2 Completed 252 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is designed to assess the effects of elagolix versus subcutaneous depot medroxyprogesterone acetate (DMPA-SC; also known as depo-provera) on bone mineral density (BMD) during treatment for 24 weeks with a subsequent 24-week post-treatment period.

Timeline

Start
2006-12-11
Primary completion
2008-11-24
Completion
2008-11-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Elagolix Small molecule 75 mg Oral
Subject Elagolix Small molecule 150 mg Oral
Comparator medroxyprogesterone acetate Other / unclassified 104 mg Subcutaneous

Indications