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A Phase II, multicenter, long-term extension study to compare the safety and efficacy of TAK-385 (10, 20, and 40 mg) following oral administration for 12 weeks or more in the treatment of endometriosis

Trial Profile

A Phase II, multicenter, long-term extension study to compare the safety and efficacy of TAK-385 (10, 20, and 40 mg) following oral administration for 12 weeks or more in the treatment of endometriosis

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 24 Sep 2018

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At a glance

  • Drugs Relugolix (Primary) ; Leuprorelin
  • Indications Endometriosis
  • Focus Adverse reactions; Biomarker; Pharmacodynamics
  • Sponsors Takeda

Most Recent Events

  • 24 May 2017 According to a Myovant Sciences media release, results from the study were presented during a poster presentation at the 2017 European Congress of Endocrinology.
  • 24 May 2017 Results published in a Myovant Sciences media release.
  • 18 May 2017 According to a Myovant Sciences media release, 24 week extension data will be presented at the 19th European Congress of Endocrinology (ECE) 2017.

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