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Clinical Trial Summary

The primary purpose of this study is to evaluate the efficacy of single oral doses of E2086 compared to placebo in the treatment of excessive daytime sleepiness (EDS) as assessed by the Maintenance of Wakefulness Test (MWT) in adult participants with narcolepsy type 1 (NT1).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06462404
Study type Interventional
Source Eisai Inc.
Contact Eisai Medical Information
Phone +1-888-274-2378
Email esi_medinfo@eisai.com
Status Not yet recruiting
Phase Phase 1
Start date June 12, 2024
Completion date February 14, 2025

See also
  Status Clinical Trial Phase
Terminated NCT04096560 - A Study of TAK-994 in Adults With Type 1 and Type 2 Narcolepsy Phase 2