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Safety, Convenience, and Tolerability of a Nightly Single Oral Dose of Extended-release Sodium Oxybate in Children
The main objectives of this study are to determine the treatment preferences of children with narcolepsy type 1 between Extended-release sodium oxybate and Non-extended-release oxybates (Sodium oxybate or a medication with the combination of Calcium, magnesium, potassium, and sodium oxybates). The study will also assess the safety, convenience, and tolerability of Extended-release sodium oxybate. Additionally, the researchers aim to assess how well Extended-release sodium oxybate works in treating narcolepsy type 1.
Age
7 - 17 years
Sex
ALL
Healthy Volunteers
No
Stanford University
Redwood City, California, United States
Start Date
October 27, 2025
Primary Completion Date
June 1, 2027
Completion Date
July 1, 2027
Last Updated
November 6, 2025
36
ESTIMATED participants
Extended-release sodium oxybate
DRUG
Non-extended-release oxybates
DRUG
Lead Sponsor
Stanford University
Collaborators
Data Source & Attribution
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