CompletedPHASE1, PHASE2NCT00637221
Open Label Study Investigating Safety and Efficacy of NPL2009 50 mg - 150 mg on Prepulse Inhibition Tests and Continuous Performance Tasks, Adults 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
- Neuropharm
- Principal Investigator
- Mike Snape, PhDNeuropharm Ltd
- Intervention
- NPL-2009(drug)
- Enrollment
- 12 enrolled
- Eligibility
- 18-45 years · All sexes
- Timeline
- 2008 – 2008
Study locations (2)
- MIND Institute, Sacramento, California, United States
- Rush University Medical Centre, Chicago, Illinois, 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.
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