The purpose of this study is to investigate the efficacy and safety after administration of TS-091 compared with placebo in patients with narcolepsy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
53
Orally taken once daily for 3 weeks
Orally taken once daily for 3 weeks
Orally taken once daily for 3 weeks
Taisho Pharmaceutical Co., Ltd selected site
Osaka and Other Japanese City, Japan
Taisho Pharmaceutical Co., Ltd selected site
Seoul and Other Korean City, South Korea
Mean sleep latency in maintenance of wakefulness test
Time frame: 3 weeks
Total score on the epworth sleepiness scale
Time frame: 3 weeks
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