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<title>Eisai Newsroom (Neurology)</title>
<link>https://media-us.eisai.com/</link>
<description>Eisai Newsroom</description>
<item>
<title>Update on FDA Priority Review of LEQEMBI® IQLIK™ (lecanemab-irmb) Subcutaneous Injection as a Starting Dose for Early Alzheimer's Disease</title>
<link>https://media-us.eisai.com/2026-05-08-Update-on-FDA-Priority-Review-of-LEQEMBI-R-IQLIK-TM-lecanemab-irmb-Subcutaneous-Injection-as-a-Starting-Dose-for-Early-Alzheimers-Disease</link>
<description></description>
<pubDate>Fri, 08 May 2026 02:30:00 -0400</pubDate>
<guid>https://media-us.eisai.com/2026-05-08-Update-on-FDA-Priority-Review-of-LEQEMBI-R-IQLIK-TM-lecanemab-irmb-Subcutaneous-Injection-as-a-Starting-Dose-for-Early-Alzheimers-Disease</guid>
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<item>
<title>Eisai to Present the Latest Data on Real-World Treatment with Lecanemab and Supporting a Standardized Framework for Treating Early Alzheimer's Disease at the 78th American Academy of Neurology's Annual Meeting</title>
<link>https://media-us.eisai.com/2026-04-09-Eisai-to-Present-the-Latest-Data-on-Real-World-Treatment-with-Lecanemab-and-Supporting-a-Standardized-Framework-for-Treating-Early-Alzheimers-Disease-at-the-78th-American-Academy-of-Neurologys-Annual-Meeting</link>
<description></description>
<pubDate>Thu, 09 Apr 2026 08:00:00 -0400</pubDate>
<guid>https://media-us.eisai.com/2026-04-09-Eisai-to-Present-the-Latest-Data-on-Real-World-Treatment-with-Lecanemab-and-Supporting-a-Standardized-Framework-for-Treating-Early-Alzheimers-Disease-at-the-78th-American-Academy-of-Neurologys-Annual-Meeting</guid>
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<item>
<title>Eisai to Begin Enrolling Phase 2 Study in Patients With Narcolepsy</title>
<link>https://media-us.eisai.com/2026-03-26-EISAI-TO-BEGIN-ENROLLING-PHASE-2-STUDY-IN-PATIENTS-WITH-NARCOLEPSY</link>
<description></description>
<pubDate>Thu, 26 Mar 2026 08:00:00 -0400</pubDate>
<guid>https://media-us.eisai.com/2026-03-26-EISAI-TO-BEGIN-ENROLLING-PHASE-2-STUDY-IN-PATIENTS-WITH-NARCOLEPSY</guid>
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<item>
<title>Results from Real-World, Long-Term Treatment Persistence with LEQEMBI® (lecanemab-irmb) in the United States Presented at AD/PD™ 2026</title>
<link>https://media-us.eisai.com/2026-03-20-Results-from-Real-World,-Long-Term-Treatment-Persistence-with-LEQEMBI-R-lecanemab-irmb-in-the-United-States-Presented-at-AD-PD-TM-2026</link>
<description></description>
<pubDate>Fri, 20 Mar 2026 12:05:00 -0400</pubDate>
<guid>https://media-us.eisai.com/2026-03-20-Results-from-Real-World,-Long-Term-Treatment-Persistence-with-LEQEMBI-R-lecanemab-irmb-in-the-United-States-Presented-at-AD-PD-TM-2026</guid>
</item>
<item>
<title>Eisai to Present the Latest Data on Long-Term, Real-World Treatment with Lecanemab at the AD/PD™ 2026 Annual Meeting</title>
<link>https://media-us.eisai.com/2026-03-10-Eisai-to-Present-the-Latest-Data-on-Long-Term,-Real-World-Treatment-with-Lecanemab-at-the-AD-PD-TM-2026-Annual-Meeting</link>
<description></description>
<pubDate>Tue, 10 Mar 2026 19:30:00 -0400</pubDate>
<guid>https://media-us.eisai.com/2026-03-10-Eisai-to-Present-the-Latest-Data-on-Long-Term,-Real-World-Treatment-with-Lecanemab-at-the-AD-PD-TM-2026-Annual-Meeting</guid>
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<item>
<title>FDA Accepts LEQEMBI® IQLIKTM (lecanemab-irmb) Supplemental Biologics License Application as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer's Disease under Priority Review</title>
<link>https://media-us.eisai.com/2026-01-25-FDA-Accepts-LEQEMBI-R-IQLIKTM-lecanemab-irmb-Supplemental-Biologics-License-Application-as-a-Subcutaneous-Starting-Dose-for-the-Treatment-of-Early-Alzheimers-Disease-under-Priority-Review</link>
<description></description>
<pubDate>Sun, 25 Jan 2026 18:30:00 -0500</pubDate>
<guid>https://media-us.eisai.com/2026-01-25-FDA-Accepts-LEQEMBI-R-IQLIKTM-lecanemab-irmb-Supplemental-Biologics-License-Application-as-a-Subcutaneous-Starting-Dose-for-the-Treatment-of-Early-Alzheimers-Disease-under-Priority-Review</guid>
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<item>
<title>Eisai Presents New Data on the Continued and Expanding Benefit of LEQEMBI® (lecanemab-irmb) Maintenance Treatment in Early Alzheimer's Disease at the Clinical Trials on Alzheimer's Disease (CTAD) Conference 2025</title>
<link>https://media-us.eisai.com/2025-12-03-Eisai-Presents-New-Data-on-the-Continued-and-Expanding-Benefit-of-LEQEMBI-R-lecanemab-irmb-Maintenance-Treatment-in-Early-Alzheimers-Disease-at-the-Clinical-Trials-on-Alzheimers-Disease-CTAD-Conference-2025</link>
<description></description>
<pubDate>Wed, 03 Dec 2025 18:10:00 -0500</pubDate>
<guid>https://media-us.eisai.com/2025-12-03-Eisai-Presents-New-Data-on-the-Continued-and-Expanding-Benefit-of-LEQEMBI-R-lecanemab-irmb-Maintenance-Treatment-in-Early-Alzheimers-Disease-at-the-Clinical-Trials-on-Alzheimers-Disease-CTAD-Conference-2025</guid>
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<item>
<title>New Data Presented at the Clinical Trials on Alzheimer's Disease (CTAD) Conference 2025 Confirms Pharmacological Effect of LEQEMBI® (lecanemab-irmb) on Neurotoxic Aβ Protofibrils in CSF</title>
<link>https://media-us.eisai.com/2025-12-02-New-Data-Presented-at-the-Clinical-Trials-on-Alzheimers-Disease-CTAD-Conference-2025-Confirms-Pharmacological-Effect-of-LEQEMBI-R-lecanemab-irmb-on-Neurotoxic-A-Protofibrils-in-CSF</link>
<description></description>
<pubDate>Tue, 02 Dec 2025 16:40:00 -0500</pubDate>
<guid>https://media-us.eisai.com/2025-12-02-New-Data-Presented-at-the-Clinical-Trials-on-Alzheimers-Disease-CTAD-Conference-2025-Confirms-Pharmacological-Effect-of-LEQEMBI-R-lecanemab-irmb-on-Neurotoxic-A-Protofibrils-in-CSF</guid>
</item>
<item>
<title>Eisai Presents New Data on Anti-Tau Antibody Etalanetug (E2814) at CTAD 2025</title>
<link>https://media-us.eisai.com/2025-12-01-Eisai-Presents-New-Data-on-Anti-Tau-Antibody-Etalanetug-E2814-at-CTAD-2025</link>
<description></description>
<pubDate>Mon, 01 Dec 2025 19:35:00 -0500</pubDate>
<guid>https://media-us.eisai.com/2025-12-01-Eisai-Presents-New-Data-on-Anti-Tau-Antibody-Etalanetug-E2814-at-CTAD-2025</guid>
</item>
<item>
<title>Eisai Completes Rolling Submission to U.S. FDA for LEQEMBI® IQLIK™ (lecanemab-irmb) Supplemental Biologics License Application as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer's Disease Under Fast Track Status</title>
<link>https://media-us.eisai.com/2025-11-25-Eisai-Completes-Rolling-Submission-to-U-S-FDA-for-LEQEMBI-R-IQLIK-TM-lecanemab-irmb-Supplemental-Biologics-License-Application-as-a-Subcutaneous-Starting-Dose-for-the-Treatment-of-Early-Alzheimers-Disease-Under-Fast-Track-Status</link>
<description></description>
<pubDate>Tue, 25 Nov 2025 07:30:00 -0500</pubDate>
<guid>https://media-us.eisai.com/2025-11-25-Eisai-Completes-Rolling-Submission-to-U-S-FDA-for-LEQEMBI-R-IQLIK-TM-lecanemab-irmb-Supplemental-Biologics-License-Application-as-a-Subcutaneous-Starting-Dose-for-the-Treatment-of-Early-Alzheimers-Disease-Under-Fast-Track-Status</guid>
</item>
<item>
<title>Eisai to Present Data on Lecanemab Continued Treatment, Subcutaneous Initiation Dosing, and Real-World Experience at the 18th Clinical Trials on Alzheimer's Disease (CTAD) Conference</title>
<link>https://media-us.eisai.com/2025-11-18-Eisai-to-Present-Data-on-Lecanemab-Continued-Treatment,-Subcutaneous-Initiation-Dosing,-and-Real-World-Experience-at-the-18th-Clinical-Trials-on-Alzheimers-Disease-CTAD-Conference</link>
<description></description>
<pubDate>Tue, 18 Nov 2025 08:00:00 -0500</pubDate>
<guid>https://media-us.eisai.com/2025-11-18-Eisai-to-Present-Data-on-Lecanemab-Continued-Treatment,-Subcutaneous-Initiation-Dosing,-and-Real-World-Experience-at-the-18th-Clinical-Trials-on-Alzheimers-Disease-CTAD-Conference</guid>
</item>
<item>
<title>LEQEMBI® IQLIK™(lecanemab-irmb) Subcutaneous Autoinjector Named to TIME's "Best Inventions of 2025"</title>
<link>https://media-us.eisai.com/2025-10-13-LEQEMBI-R-IQLIK-TM-lecanemab-irmb-Subcutaneous-Autoinjector-Named-to-TIMEs-Best-Inventions-of-2025</link>
<description></description>
<pubDate>Mon, 13 Oct 2025 19:30:00 -0400</pubDate>
<guid>https://media-us.eisai.com/2025-10-13-LEQEMBI-R-IQLIK-TM-lecanemab-irmb-Subcutaneous-Autoinjector-Named-to-TIMEs-Best-Inventions-of-2025</guid>
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<item>
<title>Eisai and Biogen Announce U.S. Availability of LEQEMBI® IQLIK™ (lecanemab-irmb) Subcutaneous Injection Maintenance Dose for Treatment of Early Alzheimer's Disease</title>
<link>https://media-us.eisai.com/2025-10-06-Eisai-and-Biogen-Announce-U-S-Availability-of-LEQEMBI-R-IQLIK-TM-lecanemab-irmb-Subcutaneous-Injection-Maintenance-Dose-for-Treatment-of-Early-Alzheimers-Disease</link>
<description></description>
<pubDate>Mon, 06 Oct 2025 16:30:00 -0400</pubDate>
<guid>https://media-us.eisai.com/2025-10-06-Eisai-and-Biogen-Announce-U-S-Availability-of-LEQEMBI-R-IQLIK-TM-lecanemab-irmb-Subcutaneous-Injection-Maintenance-Dose-for-Treatment-of-Early-Alzheimers-Disease</guid>
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<item>
<title>Anti-MTBR (microtubule binding region) Tau Antibody Etalanetug Granted FDA Fast Track Designation</title>
<link>https://media-us.eisai.com/2025-09-16-Anti-MTBR-microtubule-binding-region-Tau-Antibody-Etalanetug-Granted-FDA-Fast-Track-Designation</link>
<description></description>
<pubDate>Tue, 16 Sep 2025 19:31:00 -0400</pubDate>
<guid>https://media-us.eisai.com/2025-09-16-Anti-MTBR-microtubule-binding-region-Tau-Antibody-Etalanetug-Granted-FDA-Fast-Track-Designation</guid>
</item>
<item>
<title>Eisai Presents Clinical Study Results of Novel Orexin Receptor Agonist E2086 for Narcolepsy at World Sleep 2025</title>
<link>https://media-us.eisai.com/2025-09-08-Eisai-Presents-Clinical-Study-Results-of-Novel-Orexin-Receptor-Agonist-E2086-for-Narcolepsy-at-World-Sleep-2025</link>
<description></description>
<pubDate>Mon, 08 Sep 2025 00:01:00 -0400</pubDate>
<guid>https://media-us.eisai.com/2025-09-08-Eisai-Presents-Clinical-Study-Results-of-Novel-Orexin-Receptor-Agonist-E2086-for-Narcolepsy-at-World-Sleep-2025</guid>
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<title>Eisai to Present Latest Data on Lemborexant and Novel Orexin Receptor Agonist E2086 at The World Sleep 2025</title>
<link>https://media-us.eisai.com/2025-09-03-Eisai-to-Present-Latest-Data-on-Lemborexant-and-Novel-Orexin-Receptor-Agonist-E2086-at-The-World-Sleep-2025</link>
<description></description>
<pubDate>Wed, 03 Sep 2025 19:30:00 -0400</pubDate>
<guid>https://media-us.eisai.com/2025-09-03-Eisai-to-Present-Latest-Data-on-Lemborexant-and-Novel-Orexin-Receptor-Agonist-E2086-at-The-World-Sleep-2025</guid>
</item>
<item>
<title>Eisai Initiated Rolling Supplemental Biologics License Application to the U.S. FDA for LEQEMBI® IQLIK™ (lecanemab-irmb) as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer's Disease Under Fast Track Status</title>
<link>https://media-us.eisai.com/2025-09-02-Eisai-Initiated-Rolling-Supplemental-Biologics-License-Application-to-the-U-S-FDA-for-LEQEMBI-R-IQLIK-TM-lecanemab-irmb-as-a-Subcutaneous-Starting-Dose-for-the-Treatment-of-Early-Alzheimers-Disease-Under-Fast-Track-Status</link>
<description></description>
<pubDate>Tue, 02 Sep 2025 19:30:00 -0400</pubDate>
<guid>https://media-us.eisai.com/2025-09-02-Eisai-Initiated-Rolling-Supplemental-Biologics-License-Application-to-the-U-S-FDA-for-LEQEMBI-R-IQLIK-TM-lecanemab-irmb-as-a-Subcutaneous-Starting-Dose-for-the-Treatment-of-Early-Alzheimers-Disease-Under-Fast-Track-Status</guid>
</item>
<item>
<title>FDA Approves LEQEMBI® IQLIK™ (lecanemab-irmb) Subcutaneous Injection for Maintenance Dosing for the Treatment of Early Alzheimer's Disease</title>
<link>https://media-us.eisai.com/2025-08-29-FDA-Approves-LEQEMBI-R-IQLIK-TM-lecanemab-irmb-Subcutaneous-Injection-for-Maintenance-Dosing-for-the-Treatment-of-Early-Alzheimers-Disease</link>
<description></description>
<pubDate>Fri, 29 Aug 2025 15:58:00 -0400</pubDate>
<guid>https://media-us.eisai.com/2025-08-29-FDA-Approves-LEQEMBI-R-IQLIK-TM-lecanemab-irmb-Subcutaneous-Injection-for-Maintenance-Dosing-for-the-Treatment-of-Early-Alzheimers-Disease</guid>
</item>
<item>
<title>Two-Year Real-World Study of LEQEMBI® in the United States Presented at Alzheimer's Association International Conference (AAIC) 2025</title>
<link>https://media-us.eisai.com/2025-07-30-Two-Year-Real-World-Study-of-LEQEMBI-R-in-the-United-States-Presented-at-Alzheimers-Association-International-Conference-AAIC-2025</link>
<description></description>
<pubDate>Wed, 30 Jul 2025 11:00:00 -0400</pubDate>
<guid>https://media-us.eisai.com/2025-07-30-Two-Year-Real-World-Study-of-LEQEMBI-R-in-the-United-States-Presented-at-Alzheimers-Association-International-Conference-AAIC-2025</guid>
</item>
<item>
<title>New Data Presented at AAIC Demonstrates Investigational LEQEMBI® (lecanemab-irmb) 360 mg Subcutaneous Maintenance Dosing Could Offer a New Option for Ongoing Treatment of Early Alzheimer's Disease</title>
<link>https://media-us.eisai.com/2025-07-30-New-Data-Presented-at-AAIC-Demonstrates-Investigational-LEQEMBI-R-lecanemab-irmb-360-mg-Subcutaneous-Maintenance-Dosing-Could-Offer-a-New-Option-for-Ongoing-Treatment-of-Early-Alzheimers-Disease</link>
<description></description>
<pubDate>Wed, 30 Jul 2025 09:00:00 -0400</pubDate>
<guid>https://media-us.eisai.com/2025-07-30-New-Data-Presented-at-AAIC-Demonstrates-Investigational-LEQEMBI-R-lecanemab-irmb-360-mg-Subcutaneous-Maintenance-Dosing-Could-Offer-a-New-Option-for-Ongoing-Treatment-of-Early-Alzheimers-Disease</guid>
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<title>Early Alzheimer's Patients Continue to Benefit from Four Years of LEQEMBI® (lecanemab-irmb) Therapy New Clinical Data Presented at AAIC</title>
<link>https://media-us.eisai.com/2025-07-30-Early-Alzheimers-Patients-Continue-to-Benefit-from-Four-Years-of-LEQEMBI-R-lecanemab-irmb-Therapy-New-Clinical-Data-Presented-at-AAIC</link>
<description></description>
<pubDate>Wed, 30 Jul 2025 08:07:00 -0400</pubDate>
<guid>https://media-us.eisai.com/2025-07-30-Early-Alzheimers-Patients-Continue-to-Benefit-from-Four-Years-of-LEQEMBI-R-lecanemab-irmb-Therapy-New-Clinical-Data-Presented-at-AAIC</guid>
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<title>Eisai to Present Four-Year Efficacy and Safety Data on Continuous Treatment With Lecanemab at the Alzheimer's Association International Conference 2025</title>
<link>https://media-us.eisai.com/2025-07-21-EISAI-TO-PRESENT-FOUR-YEAR-EFFICACY-AND-SAFETY-DATA-ON-CONTINUOUS-TREATMENT-WITH-LECANEMAB-AT-THE-ALZHEIMERS-ASSOCIATION-INTERNATIONAL-CONFERENCE-2025</link>
<description></description>
<pubDate>Mon, 21 Jul 2025 19:30:00 -0400</pubDate>
<guid>https://media-us.eisai.com/2025-07-21-EISAI-TO-PRESENT-FOUR-YEAR-EFFICACY-AND-SAFETY-DATA-ON-CONTINUOUS-TREATMENT-WITH-LECANEMAB-AT-THE-ALZHEIMERS-ASSOCIATION-INTERNATIONAL-CONFERENCE-2025</guid>
</item>
<item>
<title>Eisai to Present Lecanemab Real-World Experience Data and Findings from Neurology Portfolio at the American Academy of Neurology (AAN) Annual Meeting</title>
<link>https://media-us.eisai.com/2025-03-25-EISAI-TO-PRESENT-LECANEMAB-REAL-WORLD-EXPERIENCE-DATA-AND-FINDINGS-FROM-NEUROLOGY-PORTFOLIO-AT-THE-AMERICAN-ACADEMY-OF-NEUROLOGY-AAN-ANNUAL-MEETING</link>
<description></description>
<pubDate>Tue, 25 Mar 2025 07:30:00 -0400</pubDate>
<guid>https://media-us.eisai.com/2025-03-25-EISAI-TO-PRESENT-LECANEMAB-REAL-WORLD-EXPERIENCE-DATA-AND-FINDINGS-FROM-NEUROLOGY-PORTFOLIO-AT-THE-AMERICAN-ACADEMY-OF-NEUROLOGY-AAN-ANNUAL-MEETING</guid>
</item>
<item>
<title>The Committee for Medicinal Products for Human Use (CHMP) Reaffirms Positive Opinion for Lecanemab in Early Alzheimer's Disease</title>
<link>https://media-us.eisai.com/2025-02-28-The-Committee-for-Medicinal-Products-for-Human-Use-CHMP-Reaffirms-Positive-Opinion-for-Lecanemab-in-Early-Alzheimers-Disease</link>
<description></description>
<pubDate>Fri, 28 Feb 2025 08:23:00 -0500</pubDate>
<guid>https://media-us.eisai.com/2025-02-28-The-Committee-for-Medicinal-Products-for-Human-Use-CHMP-Reaffirms-Positive-Opinion-for-Lecanemab-in-Early-Alzheimers-Disease</guid>
</item>
<item>
<title>FDA Approves LEQEMBI® (lecanemab-irmb) IV Maintenance Dosing for the Treatment of Early Alzheimer's Disease</title>
<link>https://media-us.eisai.com/2025-01-26-FDA-Approves-LEQEMBI-R-lecanemab-irmb-IV-Maintenance-Dosing-for-the-Treatment-of-Early-Alzheimers-Disease</link>
<description></description>
<pubDate>Sun, 26 Jan 2025 18:30:00 -0500</pubDate>
<guid>https://media-us.eisai.com/2025-01-26-FDA-Approves-LEQEMBI-R-lecanemab-irmb-IV-Maintenance-Dosing-for-the-Treatment-of-Early-Alzheimers-Disease</guid>
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