drugset / Trial / NCT01452685
A Long-term Extension Study of TAK-385 in the Treatment of Endometriosis
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |