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Clinical Trial Summary

The purpose of this study is to evaluate the bio-equivalence of a single oral administration of TAK-536 pediatric formulation (granules) in comparison with a TAK-536 commercial formulation (tablet) in Japanese healthy adult male participants in an open label, 2-period, 2-treatment, cross-over design.


Clinical Trial Description

The purpose of this study is to evaluate the bio-equivalence of a single oral administration of TAK-536 pediatric formulation (granules) in comparison with a TAK-536 commercial formulation (tablet) in healthy adult male participants in an open label, 2-period, 2-treatment, cross-over design. ;


Study Design


Related Conditions & MeSH terms

  • Japanese Healthy Adult Male Participants

NCT number NCT03042299
Study type Interventional
Source Takeda
Contact
Status Completed
Phase Phase 1
Start date February 10, 2017
Completion date March 11, 2017

See also
  Status Clinical Trial Phase
Completed NCT02902978 - A Single Dose Study of E6130 in Japanese Healthy Adult Male Subjects Phase 1
Completed NCT03237156 - Phase 1 TAK-906 Single and Multiple Ascending Dose Study in Japanese Healthy Male Participants Phase 1