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

Status Completed

Clinical Trial 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.

Clinical Trial Description

This study is a long-term extension study for evaluation of the safety and efficacy of TAK-385 following administration for 24 weeks (calculated from Visit 3 in the TAK-385/CCT-101 study) in participants from the Phase II dose-finding study (TAK-385/CCT-101 study). ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Endometriosis

Clinical Trial Details

NCT number	NCT01452685
Study type	Interventional
Source	Takeda
Contact
Status	Completed
Phase	Phase 2
Start date	March 2012
Completion date	December 2013

View Details

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