CompletedPhase 1NCT00634660
Safety and Tolerability Study of rAvPAL-PEG to Treat 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
- BioMarin Pharmaceutical
- Principal Investigator
- Celeste Decker, MD, M.DBioMarin Pharmaceutical
- Intervention
- rAvPAL-PEG(drug)
- Enrollment
- 25 enrolled
- Eligibility
- 16-50 years · All sexes
- Timeline
- 2008 – 2009
Study locations (8)
- Children's Memorial Hospital, Chicago, Illinois, United States
- University of Minnesota Medical Center-Fairview, Minneapolis, Minnesota, United States
- Washington University Center for Applied Research Sciences, St Louis, Missouri, United States
- Mount Sinai Medical Center, New York, New York, United States
- Oregon Health & Science University, Portland, Oregon, United States
- University of Pittsburgh, Pittsburgh, Pennsylvania, United States
- University of Utah Hospital, Salt Lake City, Utah, United States
- University of Wisconsin, Madison, Wisconsin, 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 NCT00634660 on ClinicalTrials.govOther trials for Classic phenylketonuria
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