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WKN: A3D5BP | ISIN: US28258A1079 | Ticker-Symbol: EIIA
Siehe auch EISAI CO LTD
Frankfurt
18.02.26 | 15:25
6,500 Euro
0,00 % 0,000
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MoEisai: Ministry of Health, Labour and Welfare Grants Orphan Drug Designation in Japan to Novel Orexin Receptor Agonist E2086 for Narcolepsy290TOKYO, Feb 16, 2026 - (JCN Newswire) - Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, "Eisai") announced today that it has received an orphan drug designation for its in-house discovered and...
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10.02.Eisai: Biologics License Application for Subcutaneous Formulation of "LEQEMBI(R)" (lecanemab) for the Treatment of Early Alzheimer's Disease Designated for Priority Review in China483TOKYO and CAMBRIDGE, Mass., Feb 10, 2026 - (JCN Newswire) - Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, "Eisai") and Biogen Inc. (Nasdaq: BIIB, Corporate headquarters: Cambridge, Massachusetts...
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09.02.Eisai Q3 FY2025 slides reveal 109% growth in LEQEMBI sales, strategic oncology investments11
09.02.Eisai GAAP EPS of ¥148.31, revenue of ¥619.95B; reaffirms FY outlook16
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06.02.Eisai, Henlius Strike Japan Commercialization Deal for PD-1 Antibody Serplulimab3
06.02.Leqembi starts to deliver for Eisai and Biogen16
06.02.Eisai, Henlius partner on anti-PD-1 antibody in Japan2
06.02.Eisai and Henlius Enter into Exclusive Commercial License Agreement for Anti-PD-1 Antibody Serplulimab in Japan377TOKYO and SHANGHAI, Feb 6, 2026 - (JCN Newswire) - Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, "Eisai") and Shanghai Henlius Biotech, Inc. (Headquarters: Shanghai, China, CEO: Jason Zhu...
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05.02.Eisai signs $388m deal for Japanese rights to Henlius' anti-PD-1 mAb3
05.02.Eisai and Henlius Enter into Exclusive Commercial License Agreement for Anti-PD-1 Antibody Serplulimab in Japan387TOKYO and SHANGHAI, Feb. 5, 2026 /PRNewswire/ -- Eisai Co., Ltd. ("Eisai") and Shanghai Henlius Biotech, Inc. ("Henlius") today announced the conclusion of an exclusive commercialization...
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03.02.GHIT Fund: Total Investment of Approx. USD 8.8 Million in Malaria, Tuberculosis, and NTD R&D Projects with Partners Including Mahidol University, Barcelona Institute for Global Health, and Eisai1.018TOKYO, Feb. 3, 2026 /PRNewswire/ -- The Global Health Innovative Technology (GHIT) Fund announced today a total investment of approximately JPY 1.39 billion (USD 8.8 million1) in six R&D...
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27.01.FDA to review Eisai's Leqembi Iqlik sBLA for Alzheimer's13
26.01.BioArctic: Eisai submits Marketing Authorisation Variation to EMA for intravenous maintenance dosing every four weeks with Leqembi (lecanemab)441STOCKHOLM, Sweden, Jan. 26, 2026 /PRNewswire/ -- BioArctic AB's (publ) (Nasdaq Stockholm: BIOA B) partner Eisai announced today that they have submitted a proposed Marketing Authorisation...
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26.01.Eisai and Biogen's subcutaneous Leqembi given FDA Priority Review for early Alzheimer's7
26.01.BioArctic's Partner Eisai Receives Priority Review For Leqembi Iqlik Subcutaneous Autoinjector321TOKYO (dpa-AFX) - BioArctic AB (BRCTF) announced on Monday that its partner Eisai (ESALY) has received Priority Review from the U.S. Food and Drug Administration (FDA) for the supplemental Biologics...
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26.01.FDA grants priority review for Eisai's Alzheimer's treatment autoinjector8
26.01.Eisai: FDA Accepts LEQEMBI(R) IQLIK (lecanemab-irmb) Supplemental Biologics License Application as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer's Disease under Priority Review604If approved, LEQEMBI IQLIK would be the first and only anti-amyloid treatment to offer at-home injection options for initiation and maintenance dosing for this progressive, relentless disease FDA action...
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26.01.FDA Grants Priority Review To Eisai And Biogen's SBLA For LEQEMBI Subcutaneous Autoinjector661WESTON (dpa-AFX) - Eisai Co., Ltd. (ESALY, ESALF, 4523.T) and Biogen Inc. (BIIB) announced that the U.S. Food and Drug Administration has accepted for review Eisai's Supplemental Biologics License...
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26.01.FDA accepts Eisai's autoinjector for Alzheimer's treatment under priority review5
26.01.Eisai Inc.: 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 Review1.570If approved, LEQEMBI IQLIK would be the first and only anti-amyloid treatment to offer at-home injection options for initiation and maintenance dosing for this progressive...
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