TerminatedNCT00827762
Behavioral Effects of Kuvan in Children With Mild 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
- Kuvan(drug)
- Enrollment
- 2 enrolled
- Eligibility
- 6-18 years · All sexes
- Timeline
- 2009 – 2010
Study locations (4)
- Northwestern University/Children's Memorial Hospital, Chicago, Illinois, United States
- University of Missouri, Columbia, Missouri, United States
- Washington University, St Louis, Missouri, United States
- Oregon Health & Science University, Portland, Oregon, United States
Collaborators
BioMarin Pharmaceutical · University of Missouri-Columbia · Northwestern University · Oregon Health and Science University
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 NCT00827762 on ClinicalTrials.govOther trials for Classic phenylketonuria
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