drugset / Trial / NCT01620528

A Clinical Study to Evaluate the Safety and Efficacy of Elagolix in Subjects With Moderate to Severe Endometriosis-Associated Pain

NCT01620528 ↗

Phase 3 Completed 872 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A randomized study evaluating the safety and efficacy of elagolix in the management of moderate to severe endometriosis-associated pain in adult premenopausal female participants.

Timeline

Start
2012-05-22
Primary completion
2014-11-14
Completion
2015-09-28

Outcome

Met primary endpoint

registry NUMBER Placebo: 19.6 percentage of participants NUMBER Elagolix 150 mg QD: 46.4 percentage of participants NUMBER Elagolix 200 mg BID: 75.8 percentage of participants NCT01620528 ↗

registry analysis (superiority test); Placebo vs Elagolix 150 mg QD; p < 0.001; Regression, Logistic NCT01620528 ↗

registry NUMBER Placebo: 36.5 percentage of participants NUMBER Elagolix 150 mg QD: 50.4 percentage of participants NUMBER Elagolix 200 mg BID: 54.5 percentage of participants NCT01620528 ↗

registry analysis (superiority test); Placebo vs Elagolix 200 mg BID; p < 0.001; Regression, Logistic NCT01620528 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Elagolix Small molecule 150 mg Oral
Subject Elagolix Small molecule 200 mg Oral

Indications