CompletedNCT02468570
A Phase 3 Substudy to Evaluate Executive Function in Adults With PKU Who Are Participating in the Phase 3 Study, 165-302
Studying Classic phenylketonuria
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- BioMarin Pharmaceutical
- Principal Investigator
- Debra LounsburyPrincipal Scientist/Medical Monitor
- Intervention
- Administration of CANTAB and Subject Global Assessment(other)
- Enrollment
- 9 enrolled
- Eligibility
- 18-70 years · All sexes
- Timeline
- 2015 – 2017
Study locations (4)
- University of Kentucky Medical Center, Lexington, Kentucky, United States
- University of Nebraska Medical Center, Omaha, Nebraska, United States
- University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, United States
- Oregon Health and Science University, Portland, Oregon, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT02468570 on ClinicalTrials.govOther trials for Classic phenylketonuria
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