drugset / Trial / NCT02778399

A Study to Assess the Efficacy and Safety of OBE2109 in Subjects With Endometriosis

NCT02778399

Phase 2 Completed 328 enrolled ObsEva SA
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study is to assess the efficacy and safety of a range of oral doses of OBE2109 versus placebo, in reducing endometriosis associated pain.

Timeline

Start
2016-07
Primary completion
2018-04
Completion
2019-07-01

Drugs

EvaluationDrugModalityDoseRoute
Subject linzagolix Unknown 50 mg Oral
Subject linzagolix Unknown 75 mg Oral
Subject linzagolix Unknown 100 mg Oral
Subject linzagolix Unknown 200 mg Oral

Indications