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Clinical Trial Summary

The primary purpose of this study is to assess the effect of repeated doses of DS-8500a on the single dose pharmacokinetics (PK) of rosuvastatin.

The total length of time (from screening to follow-up) for each participant is approximately 7 weeks.

It is expected that repeated oral doses of DS-8500a will not have a significant effect on the pharmacokinetics of a single dose of rosuvastatin.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Drug Pharmacokinetics in Healthy Volunteers

NCT number NCT03699774
Study type Interventional
Source Daiichi Sankyo, Inc.
Contact
Status Completed
Phase Phase 1
Start date May 12, 2015
Completion date July 6, 2015