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    Home»Health»Eisai to Present Latest Data on Lemborexant and Novel Orexin Receptor Agonist E2086 at The World Sleep 2025
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    Eisai to Present Latest Data on Lemborexant and Novel Orexin Receptor Agonist E2086 at The World Sleep 2025

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    TOKYO, Sept. 3, 2025 /PRNewswire/ — Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, “Eisai”) announced today that the company will deliver a total of 11 presentations, including clinical data on the selective orexin 2 receptor agonist (OX2R) E2086 and the latest findings on its in-house discovered orexin receptor antagonist lemborexant (product name: DAYVIGO®) at the World Sleep Congress (World Sleep 2025) to be held in Singapore from September 5 to 10.

    Key presentations include results from the Phase Ib clinical study exploring the efficacy (Proof of Mechanism) of E2086 in people diagnosed with narcolepsy type 1 (NT1) and the Phase IV clinical study (SELENADE Study) investigating the effect of lemborexant in people whose insomnia was comorbid with depressive episodes of major depressive disorder and bipolar disorder (Poster 3-133). The company will also host a symposium introducing the latest evidence on lemborexant in Asia.

    Eisai considers neurology, including sleep disorders such as insomnia and narcolepsy, as a therapeutic area of focus. Eisai strives to create innovative products in therapeutic areas with high unmet medical needs as soon as possible, and will further contribute to addressing the diverse needs of, as well as increasing the benefits provided to, those living with neurological diseases and their families.

    Oral Presentations

    Asset

    Presentation Date 

    and Time (Local)

    Title

    E2086

    Sep. 8 (Mon.)

    10:05 – 10:18 AM

    E2086, a Selective Orexin Receptor-2 Agonist, Promotes Wakefulness in
    Patients with Narcolepsy Type-1

    Poster Presentations

    Asset, Presentation Date

    Poster number, Title

    Lemborexant

    Sep. 7 (Sun.)

    Poster 1-121

    Safety and Efficacy of Lemborexant in Indian Adult Patients with Insomnia:
    A Phase 4, Prospective, Multicenter, Real-World Study

    Lemborexant

    Sep. 8 (Mon.)

    Poster 2-155

    The Effects of Lemborexant on Subjective Sleep Parameters in Insomnia
    Patients Based on Sleep State Misperception

    Lemborexant

    Sep. 8 (Mon.)

    Poster 2-158

    Consistency of Objective Results on Sleep Onset and Sleep Maintenance
    Parameters From Global Studies of Lemborexant

    Lemborexant

    Sep. 8 (Mon.)

    Poster 2-163

    The Impact of Lemborexant on Gut Microbiota Composition in Insomnia
    Treatment

    Lemborexant

    Sep. 8 (Mon.)

    Poster 2-171

    Effect of Lemborexant on Subjective Sleep Parameters in Participants with
    Insomnia Disorder: A Post Hoc Analysis of a Phase 3, Randomized Study in
    China

    Lemborexant

    Sep. 8 (Mon.)

    Poster 2-178

    The Effects of Lemborexant on Objective Sleep Parameters in Insomnia
    Patients Based on Sleep State Misperception

    Lemborexant

    Sep. 9 (Tue.)

    Poster 3-125

    Interpreting Adverse Events of Somnolence with Lemborexant in Clinical
    Trials

    Lemborexant

    Sep. 9 (Tue.)

    Poster 3-133

    Effect of Lemborexant in Patients with Insomnia Comorbid with Depressive
    Episodes (SELENADE Study)

    Lemborexant

    Sep. 9 (Tue.)

    Poster 3-149

    Efficacy and Safety of Lemborexant in South Korean Participants with
    Insomnia Disorder: Results from a Randomized Phase 2 Bridging Study

    Lemborexant

    Sep. 9 (Tue.)

    Poster 3-150

    One-Month Follow-Up Results of Patient-Reported Outcomes for
    Lemborexant treatment in Chinese Patients with Insomnia (PROEM): a
    Multicenter, Prospective, Real-world Observational Study

    Eisai-Sponsored Symposium: RISE – Regional Insights in Sleep Excellence
    Sep.8 (Mon.) 12:45-13:45 PM

    Title

    Evolving National Guidelines: The 2025 Thailand/Thai Framework for Insomnia Management

    Real-World Use of Lemborexant in Japan: Insights from the SELENADE Study

    This release discusses investigational uses of agents in development and is not intended to convey conclusions about efficacy or safety. There is no guarantee that such investigational agent will successfully complete clinical development or gain health authority approval.

    MEDIA CONTACTS

    Eisai Co., Ltd.

    Public Relations Department,

    TEL: +81-(0)3-3817-5120

     

    Eisai Europe, Ltd.

    EMEA Communications Department

    + 44 (0) 797 487 9419

     

    Eisai Inc. (U.S.)

    Libby Holman

    + 1-201-753-1945

    [Notes to editors]

    1. About lemborexant (product name: DAYVIGO)
      Lemborexant, an orexin receptor antagonist, is Eisai’s in-house discovered and developed small molecule that inhibits orexin neurotransmission by binding competitively to the two subtypes of orexin receptors (orexin receptor 1 and 2). Fast on/off receptor kinetics of lemborexant to orexin receptors may influence lemborexant’s potential to facilitate improvements in sleep onset and maintenance with minimal morning residual effects. It has been approved for the treatment of insomnia in more than 25 countries including Japan, the United States, China, Canada, Australia and countries in Asia and the Middle East.
    2. About E2086
      E2086 is Eisai’s in house discovered novel selective orexin 2 receptor agonist. Nonclinical studies have demonstrated statistically significant increases in time spent awake and significant reductions in rates of cataplexy. Individuals with a deficiency of orexin demonstrate excessive daytime sleepiness (EDS), as exemplified by patients with narcolepsy Type 1, demonstrate a loss of orexinergic neurons, and low cerebrospinal fluid (CSF) orexin levels. E2086 has the potential to improve patients’ symptoms by enhancing orexin receptor activity.
    3. About narcolepsy
      Narcolepsy is a chronic sleep disorder with that is characterized by EDS. Narcolepsy is classified into two subtypes, type 1 (narcolepsy with cataplexy) and type 2 (narcolepsy without cataplexy). Disease burden is high because of problems with fatigue, cognition, and persistence of residual symptoms despite treatment.1

    SOURCE Eisai Inc.

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