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Clinical Trial Summary

This study is an international, multi-center, randomized, double-blind, placebo-controlled, two-treatment, two-period cross-over study to evaluate the pharmacodynamics, safety, tolerability and pharmacokinetics of a single oral dose of CDX-6114 in patients with phenylketonuria (PKU).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04085666
Study type Interventional
Source Nestlé
Contact
Status Completed
Phase Phase 1
Start date June 1, 2019
Completion date August 30, 2020

See also
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