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Clinical Trial Summary

The primary objectives of the study are to evaluate the safety, tolerability and pharmacokinetics of A4250 after single or multiple oral doses in healthy subjects. In addition, will evaluate A4250 in combination with cholestyramine.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02963077
Study type Interventional
Source Ipsen
Contact
Status Completed
Phase Phase 1
Start date July 2013
Completion date May 2014

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