This is a randomized, placebo-controlled, double-blind, multiple cohort, fixed-dose multiple crossover, dose-finding study of oral BTD-001 in adult patients with IH or Narcolepsy without cataplexy (Type 2).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
120
Sleep Disorders Center of Alabama
Birmingham, Alabama, United States
Efficacy Epworth Sleepiness Scale
Epworth Sleepiness Scale
Time frame: After 14 days per treatment
Efficacy Maintenance of Wakefulness Test
Maintenance of Wakefulness Test
Time frame: After 14 days per treatment
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