CompletedPhase 3NCT01325220
Efficacy and Safety Study of STX209 (Arbaclofen) for the Treatment of Social Withdrawal in Children With Fragile X Syndrome
Studying Fragile X syndrome
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
- Seaside Therapeutics, Inc.
- Principal Investigator
- Paul Wang, M.D.Seaside Therapeutics, Inc.
- Intervention
- arbaclofen(drug)
- Enrollment
- 172 enrolled
- Eligibility
- 5-11 years · All sexes
- Timeline
- 2011
Study locations (28)
- Southwest Autism Research & Resource Center, Phoenix, Arizona, United States
- Miller Children's Hospital, Long Beach, California, United States
- University of California-Davis, M.I.N.D. Institute, Sacramento, California, United States
- Psychiatric Centers at San Diego, San Diego, California, United States
- University of Colorado Denver, Children's Hospital, Aurora, Colorado, United States
- University of Miami, Mailman Center for Child Development, Miami, Florida, United States
- Lake Mary Pediatrics, Orange City, Florida, United States
- Emory University School of Medicine, Decatur, Georgia, United States
- Rush University Medical Center, Chicago, Illinois, United States
- Kansas University Clinical Research Center, Fairway, Kansas, United States
- Kennedy Krieger Institute, Baltimore, Maryland, United States
- University of Massachusetts, Worcester, Massachusetts, United States
- Children's Hospital of Michigan, Detriot, Michigan, United States
- University of Missouri, Thompson Research Center for Autism & Neurodevelopmental Disorders, Columbia, Missouri, United States
- Seaver Autism Center, Mount Sinai Medical Center, New York, 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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