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WKN: A3D5BP | ISIN: US28258A1079 | Ticker-Symbol: EIIA
Siehe auch EISAI CO LTD
Frankfurt
21.08.26 | 15:25
6,150 Euro
-1,60 % -0,100
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Pharma
Aktienmarkt
JAPAN
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EISAI CO LTD ADR Chart 1 Jahr
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DiEurofarma partners with Eisai to bring insomnia drug to Brazil4
MoEurofarma brings Eisai's insomnia drug Dayvigo to Brazil2
EISAI CO LTD ADR Aktie jetzt für 0€ handeln
06.08.Nuvation Bio outlines $30M Eisai milestone timing while expanding safusidenib studies with PFS readouts expected in 202925
03.08.Eisai Q1 FY2026 slides: 3L products drive 15.6% revenue growth4
03.08.Eisai Q1 FY2026 slides: revenue tops forecast, stock falls 3.6%2
03.08.Eisai übertrifft Umsatzprognose in Q1 2026, Aktie gibt dennoch um 3,6 % nach2
03.08.Earnings Call: Eisai übertrifft Umsatzprognose in Q1 2026, Aktie gibt dennoch um 3,6 % nach2
03.08.Eisai GAAP EPS of ¥64.71, revenue of ¥234.3B; updates FY 2026 outlook8
03.08.Eisai Q1 Net Income Rises267BRUSSELS/FRANKFURT/PARIS (dpa-AFX) - Eisai Co. (4523.T, EII.SG) reported that its first-quarter profit attributable to owners of the parent increased 26.0% to 18.24 billion yen from 14.47 billion...
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29.07.Eisai and CORE Biomedicine agree on global licence for oncology pipeline4
27.07.Pfizer and Eisai Commence Co-promotion of "NURTEC(R)" for the Acute Treatment and Prophylaxis (Preventive Treatment) of Migraine970TOKYO, July 27, 2026 - (JCN Newswire) - Pfizer Japan Inc. (Headquarters: Tokyo, President and Representative Director: Hiroo Igarashi, "Pfizer") and Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo...
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20.07.Eisai: Marketing Authorization Application for In-house Developed Insomnia Drug Lemborexant Accepted for Evaluation by European Medicines Agency (EMA)960TOKYO, July 17, 2026 - (JCN Newswire) - Eisai Co., Ltd. announced today that the European Medicines Agency (EMA) has accepted for evaluation a marketing authorization application (MAA) for its in-house-discovered...
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18.07.EMA accepts Eisai application for insomnia drug lemborexant3
15.07.Eisai: LEQEMBI(R) Real-World LEADER Study Presented at AAIC(R) 2026 Finds Over 75% of Early Alzheimer's Patients Enrolled in the Study Remained Stable and Nearly 7% Improved Over an Average of 17 Months of Treatment665Real-World Findings Support Long-Term Benefits of Continuous Treatment with LEQEMBI and Provide Important Insights into Treatment Experience Outside of a Clinical Trial SettingTOKYO and CAMBRIDGE, Mass....
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15.07.Alzheimer-Therapie: FDA genehmigt wöchentliche subkutane Lecanemab-Injektion von Eisai und Biogen29
15.07.Eisai: FDA Approves LEQEMBI IQLIK(R) (lecanemab-irmb) Subcutaneous Injection as an Initiation Dose for Early Alzheimer's Disease514LEQEMBI IQLIK is a first-of-its-kind anti-amyloid treatment worldwide, offering at-home dosing for initiation and maintenance (approved in the U.S.)U.S. launch of LEQEMBI IQLIK as an initiation dose...
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15.07.Eisai Presents Latest Findings Showed Etalanetug Reduced Alzheimer's Disease Tau Tangle-Specific Plasma Biomarker MTBR-tau243 at Alzheimer's Association International Conference(R) (AAIC(R)) 2026489Measuring the plasma eMTBR-tau243 biomarker may serve as a practical, less invasive method of capturing Alzheimer's disease-specific pathological changes and may play an important role in etalanetug's...
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15.07.Biogen and Eisai's Leqembi study shows nearly 83% of early Alzheimer's patients remained stable or improved16
14.07.Eisai, Biogen Report Study Showing Long-Term Benefits Of LEQEMBI In Early Alzheimer's Disease554WESTON (dpa-AFX) - Eisai Co Ltd (ESALY.PK) and Biogen Inc. (BIIB) announced on Tuesday new real-world data showing that 82.5 percent of patients with early Alzheimer's disease remained stable...
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14.07.Eisai, Biogen report real-world Alzheimer's drug study results5
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