CompletedPhase 3NCT00838435
Effect of Kuvan on Neurocognitive Function, Blood Phenylalanine Level, Safety, and Pharmacokinetics in Children With PKU
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
- Joshua Lilienstein, M.D., M.DBioMarin Pharmaceutical
- Intervention
- sapropterin dihydrochloride(drug)
- Enrollment
- 95 enrolled
- Eligibility
- 6 years · All sexes
- Timeline
- 2009 – 2018
Study locations (19)
- La Jolla, California, United States
- Orange, California, United States
- Tampa, Florida, United States
- Chicago, Illinois, United States
- Boston, Massachusetts, United States
- Kansas City, Missouri, United States
- Cleveland, Ohio, United States
- Columbus, Ohio, United States
- Hershey, Pennsylvania, United States
- Nashville, Tennessee, United States
- Salt Lake City, Utah, United States
- Milwaukee, Wisconsin, United States
- Edmonton, Alberta, Canada
- Vancouver, British Columbia, Canada
- Winnipeg, Manitoba, Canada
- +4 more locations on ClinicalTrials.gov
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 NCT00838435 on ClinicalTrials.govOther trials for Classic phenylketonuria
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