CompletedPhase 2NCT00925054
Dose-Finding Study to Evaluate the Safety, Efficacy, & Tolerability of Multiple Doses of rAvPAL-PEG in Subjects 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
- Ari Gershman, MD, M.DBioMarin Pharmaceutical
- Intervention
- rAvPAL-PEG 0.001 mg/kg(drug)
- Enrollment
- 40 enrolled
- Eligibility
- 16-55 years · All sexes
- Timeline
- 2009 – 2015
Study locations (11)
- The Children's Hospital, Aurora, Colorado, United States
- Emory Universty, Decatur, Georgia, United States
- 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
- Albany Medical Center, Albany, New York, United States
- Mount Sinai School of Medicine, New York, New York, United States
- Akron Children's Hospital, Akron, Ohio, United States
- Oregon Health & Science University, Portland, Oregon, United States
- University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States
- University of Utah Hospital, Salt Lake City, Utah, 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 NCT00925054 on ClinicalTrials.govOther trials for Classic phenylketonuria
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