drugset / Trial / NCT01452685

A Long-term Extension Study of TAK-385 in the Treatment of Endometriosis

NCT01452685

Phase 2 Completed 397 enrolled Takeda
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to compare the long term safety and efficacy of TAK-385, once daily (QD) following continued administration in participants who completed a Phase II dose-finding study.

Timeline

Start
2012-03
Primary completion
2013-12
Completion
2013-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Leuprolide Other / unclassified 3.75 mg Subcutaneous
Subject Relugolix Small molecule 10 mg Oral
Subject Relugolix Small molecule 20 mg Oral
Subject Relugolix Small molecule 40 mg Oral

Indications