Natural History Clinical Study in Adult PKU
NCT04768348 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 7
Last updated 2023-08-25
Summary
The objective of this study is to characterize the natural history of phenylketonuria (PKU) due to phenylalanine hydroxylase (PAH) deficiency in adults through prospective collection of clinical, cognitive, and quality of life assessments.
Conditions
- Phenylketonurias
- PKU
Sponsors & Collaborators
-
Homology Medicines, Inc
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Max Age
- 55 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-04-20
- Primary Completion
- 2023-02-01
- Completion
- 2023-08-01
Countries
- United States
Study Locations
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