Clinical trial
Open-Label Safety Study of a 1-Year 20 mg Dose Regimen of Tasimelteon for Treatment of Non-24-Hour-Sleep-Wake Disorder (N24HSWD) in Blind Individuals With No Light Perception
NCT01218789 is registered in ClinicalTrials.gov with Vanda Pharmaceuticals as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Open-Label Safety Study of a 1-Year 20 mg Dose Regimen of Tasimelteon for Treatment of Non-24-Hour-Sleep-Wake Disorder (N24HSWD) in Blind Individuals With No Light Perception
- Lead sponsor
- Vanda Pharmaceuticals
- Phase
- Phase 3
- Overall status
- Unknown status
- Start date
- October 28, 2010
- Completion date
- December 5, 2024
- Enrollment
- 140 (estimated)
- Sites
- 7
Conditions
As the registry lists them; a condition with its own page is linked.
non 24 hour sleep wake disorder