CompletedPhase 2NCT00724048
A Study of Pridopidine (ACR16) for the Treatment of Participants With Huntington's Disease
Studying Huntington disease
Last synced from ClinicalTrials.gov
ℹ
Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Teva Branded Pharmaceutical Products R&D, Inc.
- Principal Investigator
- Teva Medical ExpertTeva Branded Pharmaceutical Products R&D, Inc.
- Intervention
- ACR16(drug)
- Enrollment
- 227 enrolled
- Eligibility
- 30 years · All sexes
- Timeline
- 2008 – 2010
Study locations (28)
- University of Alabama at Birmingham, Birmingham, Alabama, United States
- University of California, San Diego, California, United States
- Colorado Neurological Institute, Littleton, Colorado, United States
- University of South Florida, Tampa, Florida, United States
- Rush University Medical Center, Chicago, Illinois, United States
- Indiana University School of Medicine, Indianapolis, Indiana, United States
- University of Iowa, Iowa City, Iowa, United States
- University of Maryland School of Medicine, Baltimore, Maryland, United States
- Johns Hopkins University, Baltimore, Maryland, United States
- Massachusetts General Hospital, Charlestown, Massachusetts, United States
- Struthers Parkinson's Center, Saint Louis Park, Minnesota, United States
- Washington University School of Medicine, St Louis, Missouri, United States
- Albany Medical College, Albany, New York, United States
- North Shore-LIJ Health System, Manhasset, New York, United States
- University of Rochester, Rochester, New York, United States
- +13 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.
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