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PANDA: PKU Amino Acid Evaluation | Clinical Trials | Clareo Health

COMPLETEDNCT04086511

PANDA: PKU Amino Acid Evaluation

Phenylketonuria (PKU) is a rare inherited metabolic disorder, where subjects are born with a genetic deficiency in the phenylalanine hydroxylase enzyme (PAH), which leaves them unable to convert Pheny...

Lead sponsor: Nutricia Research•2 locations•View source on ClinicalTrials.gov

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: June 2, 2023Terms

Trial snapshot

StatusCOMPLETED

Phase—

Enrollment37

Start dateSep 2019

Last updatedJun 2, 2023

Condition

Phenylketonuria (PKU)

Locations shown

Dr. P. Verloo

Ghent

Birmingham Children's Hospital

Birmingham

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: June 2, 2023Data synced to Clareo: May 25, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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