Eisai, Inc._E2086-G000-202_140993-01_Narcolepsy (140993-01)

  • STATUS
    Recruiting
  • sponsor
    Eisai, Inc.
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Updated on 24 June 2026

Summary

To identify the optimal doses of E2086 compared to placebo in subjects with narcolepsy for reduction of excessive daytime sleepiness (EDS) as assessed by Mean Sleep Latency (MSL)

Description

A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Efficacy and Safety of E2086 in Adults with Narcolepsy. Multicenter, global at approximately 65 sites in North America, Europe, and Asia.  Two cohorts for NT1 & NT2.  320 screened to provide 64 randomized subjects. 32 subjects with NT1 and approximately 32 subjects with NT2.

Details
Condition Narcolepsy; Excessive daytime sleepiness (EDS) as assessed by Mean Sleep Latency (MSL); Weekly Cataplexy Rate (WCR)
Age 18years or above
Clinical Study IdentifierEisai, Inc.
SponsorEisai, Inc.
Last Modified on24 June 2026

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