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Clinical Trial Summary

The primary objectives of the study are to assess the relative bioavailability of the BIIB074 direct compression formulation (DCF) to the BIIB074 roller compaction formulation (RCF) and to determine the effect of a high-fat meal on the pharmacokinetics (PK) of the BIIB074 DCF. The secondary objective of the study is to assess the safety and tolerability of BIIB074 administered as the DCF following single oral dose administration in healthy participants.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02951221
Study type Interventional
Source Biogen
Contact
Status Completed
Phase Phase 1
Start date December 2016
Completion date February 2017

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