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WKN: A3D5BP | ISIN: US28258A1079 | Ticker-Symbol: EIIA
Siehe auch EISAI CO LTD
Frankfurt
18.12.25 | 15:29
5,950 Euro
+1,71 % +0,100
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DiEisai Rated "A", the Highest Rating by CDP in Both Climate Change and Water Security Categories for the Second Consecutive Year215TOKYO, Dec 11, 2025 - (JCN Newswire) - Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, "Eisai") has announced that it has been selected for the highest-rated "A" List in the fields of Climate...
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DiEisai: "LEQEMBI(R)" (lecanemab) for the Treatment of Early Alzheimer's Disease Included in China's Commercial Insurance Innovative Drug List242TOKYO and CAMBRIDGE, Mass., Dec 9, 2025 - (JCN Newswire) - Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, "Eisai") and Biogen Inc. (Nasdaq: BIIB, Corporate headquarters: Cambridge, Massachusetts...
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08.12.Eisai: New Data Presented at CTAD 2025 Confirms Pharmacological Effect of LEQEMBI(R) (lecanemab-irmb) on Neurotoxic Aβ Protofibrils in CSF460TOKYO and CAMBRIDGE, Mass., Dec 3, 2025 - (JCN Newswire) - Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, "Eisai") and Biogen Inc. (Nasdaq: BIIB, Corporate headquarters: Cambridge, Massachusetts...
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08.12.Eisai Presents New Data on the Continued and Expanding Benefit of LEQEMBI(R) (lecanemab-irmb) Maintenance Treatment in Early Alzheimer's Disease at CTAD 2025351- Long-term LEQEMBI treatment suggests potential to delay disease progression from MCI to moderate Alzheimer's disease by up to 8.3 years in low-amyloid group who started treatment at an early stage-...
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04.12.Eisai And Biogen Report Long-Term Benefits Of LEQEMBI In Early Alzheimer's Disease485WESTON (dpa-AFX) - Eisai Co., Ltd. and Biogen Inc. announced new findings on the continued and expanding benefit of LEQEMBI (lecanemab-irmb) maintenance treatment in early Alzheimer's disease...
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03.12.Eisai Presents New Data on Anti-Tau Antibody Etalanetug (E2814) at CTAD 2025348Etalanetug demonstrated reduction of eMTBR-tau243, a novel CSF and plasma biomarker that specifically reflects tau tangle pathology, in phase Ib/II studyTOKYO, Dec 2, 2025 - (JCN Newswire) - Eisai Co....
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02.12.Regulatory tracker: Eisai finalizes FDA filing for subcutaneous Leqembi starter dose5
02.12.Eisai: Etalanetug Demonstrates Reduction Of EMTBR-tau243 In Phase Ib/II Alzheimer's Study381WESTON (dpa-AFX) - Eisai Co., Ltd. announced new data on its anti-tau antibody etalanetug at the 18th Clinical Trials on Alzheimer's Disease (CTAD) Conference. Etalanetug is designed to bind...
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01.12.Eisai submits new drug application for subcutaneous Leqembi in Japan9
01.12.Eisai seeks PMDA approval for subcutaneous Leqembi in Japan5
01.12.Eisai Submits New Drug Application for Subcutaneous Formulation of "LEQEMBI(R)" for the Treatment of Early Alzheimer's Disease in Japan398If approved, lecanemab would be the first and only anti-amyloid treatment in Japan to offer an at-home injection from the initiation of treatment for this progressive, relentless disease TOKYO and CAMBRIDGE...
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28.11.Biogen, Eisai File In Japan To Make Leqembi A Weekly At-Home Alzheimer's Shot8
28.11.Eisai Announces Filing Of New Drug Application For Leqembi In Japan377BRUSSELS/FRANKFURT/PARIS (dpa-AFX) - BioArctic AB's (BIOA-B.ST) partner Eisai (4523.T) announced that they have filed a new drug application for Leqembi or lecanemab for a subcutaneous formulation...
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28.11.Biogen Inc.: Eisai Submits New Drug Application for Subcutaneous Formulation of "LEQEMBI" for the Treatment of Early Alzheimer's Disease in Japan345TOKYO and CAMBRIDGE, Mass., Nov. 27, 2025 (GLOBE NEWSWIRE) -- Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, "Eisai") and Biogen Inc. (Nasdaq: BIIB, Corporate headquarters: Cambridge, Massachusetts...
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26.11.Eisai Completes Rolling Submission to US FDA for LEQEMBI(R) IQLIK (lecanemabirmb) Supplemental Biologics License Application as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer's Disease Under Fast Track Status391LEQEMBI IQLIK, if approved for initiation dosing, would be the first and only anti-amyloid treatment to offer at-home injection from the start of therapy to help patients and care partners treat this...
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25.11.Biogen Inc.; Eisai Co., Ltd.: Eisai Completes Rolling Submission to US 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 ...4
25.11.Eisai Inc.: 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 ...209LEQEMBI IQLIK, if approved for initiation dosing, would be the first and only anti-amyloid treatment to offer at-home injection from the start of therapy to help...
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19.11.Biogen and Eisai receive MHRA approval for updated dosing of early Alzheimer's treatment19
17.11.Eisai: "LEQEMBI(R)" (lecanemab) IV Maintenance Dosing for the Treatment of Early Alzheimer's Disease Approved in the United Kingdom351TOKYO and CAMBRIDGE, Mass., Nov 17, 2025 - (JCN Newswire) - Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, "Eisai") and Biogen Inc. (Nasdaq: BIIB, Corporate headquarters: Cambridge, Massachusetts...
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14.11.Eisai and Biogen report Leqembi's MHRA approval for Alzheimer's4
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