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Clinical Trial Summary

This study is to assess the bioequivalence of a test formulation of vadadustat (A) compared to a reference formulation of vadadustat (B)


Clinical Trial Description

This is a randomized, open-label, single-dose, two-period crossover study in healthy adults to assess the bioequivalence of a test formulation of vadadustat compared to the reference formulation of vadadustat. Blood samples for vadadustat PK will be collected at pre-dose (0 hour) and at 0.5, 1, 1.5, 2, 3, 4, 6, 9, 12, 18, 24, 32, 40, and 48 hours post-dose. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03639155
Study type Interventional
Source Akebia Therapeutics
Contact
Status Completed
Phase Phase 1
Start date April 12, 2018
Completion date May 23, 2018

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