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ong-Term Study of CN-801 in patients with idiopathic hypersomnia

Phase 3
Conditions
Idiopathic hypersomnia
Registration Number
JPRN-jRCT2080222564
Lead Sponsor
Alfresa Pharma Corporation
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Patients diagnosed with idiopathic hypersomnia based on the International Classification of Sleep Disorders, second edition (ICSD-2) and who have completed the preceding double-blind comparative study

Exclusion Criteria

Patients with narcolepsy, restless legs syndrome, periodic limb movement disorder, or sleep apnea syndrome
Patients working irregular shifts or night shifts
Patients with chronic sleep deprivation or patients with extremely irregular bed times

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Safty, Efficacy (Japanese version of the Epworth Sleepiness Scale)
Secondary Outcome Measures
NameTimeMethod
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