Clin2
NCT07551921Likely a fitRecruiting

Blood Test Validation for Phenylketonuria Monitoring

Phenylketonuria (PKU) and Hyperphenylalaninemia

Part of Brain & nervous system, Genetic & congenital, Hormones & metabolism clinical trials.

This study tests a new fingerstick blood test (PheCheck™) designed to help monitor phenylketonuria (PKU), a rare condition affecting how the body processes a protein called phenylalanine. If you or your child has PKU and are already being monitored for it, this study may help improve how your care team tracks the condition.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
60 people
Ages
1 year and older
Study type
Observational

Who can take part

  • You or your child must be at least 1 year old and able to have a small blood sample taken from a fingerstick
  • You must have been diagnosed with phenylketonuria (PKU)—including classical PKU, mild PKU, variant PKU, or high phenylalanine levels
  • You must already be regularly monitored for PKU by a healthcare provider
  • You or your legal guardian must be able to read and understand study instructions
  • You must sign an informed consent form (or have your guardian sign for you if you're a minor)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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