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
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https://search.vivli.org/doiLanding/studies/PR00009883/isLanding
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资源简介:
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.
提供机构:
Vivli
创建时间:
2024-03-14



