This is a double-blind, randomized, two-period crossover study to evaluate the efficacy and safety of a single oral dose of tasimelteon and matching placebo in male and female subjects with DSWPD and the CRY1Δ11 variant.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
60
Oral capsule
Oral capsule
Vanda Investigational Site
Çankaya, Ankara, Turkey (Türkiye)
RECRUITINGLatency to Persistent Sleep, as measured by polysomnography.
Time frame: Two Nights
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