Dataset from A Randomized, Open-label, 2×2 Crossover, Phase I Study to Evaluate the Bioequivalence of Single Oral Dose of TAK-536 Pediatric Formulations and TAK-536 Commercial Tablet in Healthy Adult Male Subjects
收藏NIAID Data Ecosystem2026-05-10 收录
下载链接:
https://doi.org/10.25934/PR00007570
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资源简介:
The purpose of this study is to evaluate the bioequivalence of a single oral dose of 2
different drug forms of TAK-536 pediatric formulation and a single oral dose of TAK-536
commercial tablet in healthy Japanese adult male participants.
创建时间:
2025-10-01



