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WKN: A3D5BP | ISIN: US28258A1079 | Ticker-Symbol: EIIA
Siehe auch EISAI CO LTD
Frankfurt
12.05.26 | 15:25
5,850 Euro
0,00 % 0,000
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FrEisai, Biogen face delay to subcutaneous Leqembi2
FrEisai, Biogen Say FDA Extends Review Of LEQEMBI IQLIK As A Starting Dose For Early AD321WESTON (dpa-AFX) - Eisai Co. Ltd (ESALY.PK) and Biogen Inc. (BIIB) on Friday said the U.S. Food and Drug Administration has extended by three months the review of LEQEMBI IQLIK as a starting...
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EISAI CO LTD ADR Aktie jetzt für 0€ handeln
FrFDA verlängert Prüffrist für Alzheimer-Medikament von Eisai und Biogen15
FrFDA extends review period for Eisai, Biogen Alzheimer's drug4
FrEisai Co., Ltd.: Update on FDA Priority Review of LEQEMBI IQLIK (lecanemab-irmb) Subcutaneous Injection as a Starting Dose for Early Alzheimer's Disease750TOKYO and CAMBRIDGE, Mass., May 8, 2026 /PRNewswire/ -- Eisai Co., Ltd. and Biogen Inc. (Nasdaq: BIIB) today announced that the U.S. Food and Drug Administration...
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22.04.GHIT Fund: Total Investment of Approx. USD 8.5 Million in Malaria and NTD R&D Projects With Partners Including MMV, GSK, Tanabe Pharma, Eisai and DNDi944TOKYO, April 22, 2026 /PRNewswire/ -- The Global Health Innovative Technology (GHIT) Fund announced today a total investment of approximately JPY 1.37 billion (USD 8.5 million1) in five R&D...
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21.04.Tortugas debuts with $106M and brain drugs from Hansoh, Eisai3
21.04.Merck, Eisai trial fails to improve kidney cancer treatment14
21.04.MSD, Eisai report setback in first-line kidney cancer trial9
21.04.Merck & Co., Inc., Rahway, NJ, USA and Eisai Provide Update on Phase 3 LITESPARK-012 Trial Evaluating First-Line Combination Treatments for Certain Patients With Advanced Renal Cell Carcinoma (RCC)521TOKYO and RAHWAY, N.J., Apr 21, 2026 - (JCN Newswire) - Merck & Co., Inc., Rahway, NJ, USA (known as MSD outside of the United States and Canada), and Eisai (Headquarters: Tokyo, CEO: Haruo Naito) today...
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21.04.Merck, Eisai face setback in late-stage trial for Keytruda regimen in kidney cancer11
01.04.Nuvation Bio Inc. (NUVB) and Eisai Get EMA Validation for Taletrectinib5
27.03.Eisai: Application Submitted for LENVIMA(R) (lenvatinib) in Japan Seeking Approval of Additional Dosage and Administration for Combination with WELIREG(R) (belzutifan) for Renal Cell Carcinoma that has Progressed After Chemotherapy655TOKYO, Mar 27, 2026 - (JCN Newswire) - Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, "Eisai") and MSD K.K. (Headquarters: Tokyo, Representative Director: Prashant Nikam, "MSD"), a subsidiary...
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27.03.Eisai and Nuvation Bio Announce Marketing Authorisation Application for Taletrectinib for the Treatment of Advanced ROS1-Positive Non-Small Cell Lung Cancer Validated by the European Medicines Agency610- The Marketing Authorisation Application (MAA) has been validated and accepted for full approval consideration with a standard review timeline- Additional filings are planned for the U.K., Canada and...
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26.03.Nuvation Bio, Eisai application for taletrectinib for NSCLC accepted by EMA5
26.03.Eisai startet Phase-2-Studie für Narkolepsie-Wirkstoff E20867
25.03.Eisai and Biogen's new data shows Alzheimer's patients choose to stay on Leqembi long-term17
23.03.Eisai: Results from Real-World, Long-Term Treatment Persistence with LEQEMBI(R) (lecanemab-irmb) in the United States Presented at AD/PD 2026497Real-World LEQEMBI Data Shows Patients Choose to Stay on Long-Term TreatmentTOKYO and CAMBRIDGE, Mass., Mar 23, 2026 - (JCN Newswire) - Eisai Co., Ltd. and Biogen Inc. announced today that new real-world...
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20.03.Eli Lilly, Biogen/Eisai win U.K. review for use of Alzheimer's drugs in NHS9
19.03.Eisai: Regarding Discontinuation of Administration of "Tazverik(R) Tablets 200mg" (tazemetostat hydrobromide)471TOKYO, Mar 19, 2026 - (JCN Newswire) - Eisai Co., Ltd. announced today that the administration of the anticancer agent EZH2 inhibitor "Tazverik(R) Tablets 200 mg" (generic name: tazemetostat hydrobromide)...
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