CompletedNCT00730080
Sapropterin in Individuals With Phenylketonuria
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
- Washington University School of Medicine
- Principal Investigator
- Desiree White, Ph.D.Washington University School of Medicine
- Intervention
- Sapropterin (Kuvan)(drug)
- Enrollment
- 45 enrolled
- Eligibility
- 6-50 years · All sexes
- Timeline
- 2008 – 2018
Study locations (1)
- Washington University, St Louis, Missouri, United States
Collaborators
BioMarin Pharmaceutical · University of Missouri-Columbia
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.
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