Anzeige
Mehr »
Samstag, 07.02.2026 - Börsentäglich über 12.000 News
Der Shakeout: Silber hat genau das getan, was echte Bullenmärkte immer tun - es hat die Touristen abgeschüttelt
Anzeige

Indizes

Kurs

%
News
24 h / 7 T
Aufrufe
7 Tage

Aktien

Kurs

%
News
24 h / 7 T
Aufrufe
7 Tage

Xetra-Orderbuch

Fonds

Kurs

%

Devisen

Kurs

%

Rohstoffe

Kurs

%

Themen

Kurs

%

Erweiterte Suche

WKN: 855526 | ISIN: JP3160400002 | Ticker-Symbol: EII
Tradegate
06.02.26 | 18:19
23,840 Euro
-1,04 % -0,250
Branche
Pharma
Aktienmarkt
NIKKEI-225
1-Jahres-Chart
EISAI CO LTD Chart 1 Jahr
5-Tage-Chart
EISAI CO LTD 5-Tage-Chart
RealtimeGeldBriefZeit
23,72024,50010:16
23,90024,25006.02.

Aktuelle News zur EISAI Aktie

Aktienalarm. Jetzt kostenlos anmelden!

E-Mail
Aktivieren
  • Alle
  • Pressemitteilungen
  • Empfehlungen
  • Chartanalysen
  • Berichte
ZeitAktuelle Nachrichten
Sprache: Alle DE EN
LeserMedien
EISAI Aktie jetzt für 0€ handeln
FrEisai, Henlius Strike Japan Commercialization Deal for PD-1 Antibody Serplulimab3
FrLeqembi starts to deliver for Eisai and Biogen13
FrEisai, Henlius partner on anti-PD-1 antibody in Japan2
FrEisai and Henlius Enter into Exclusive Commercial License Agreement for Anti-PD-1 Antibody Serplulimab in Japan263TOKYO 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...
► Artikel lesen
DoEisai signs $388m deal for Japanese rights to Henlius' anti-PD-1 mAb3
DoEisai and Henlius Enter into Exclusive Commercial License Agreement for Anti-PD-1 Antibody Serplulimab in Japan311TOKYO and SHANGHAI, Feb. 5, 2026 /PRNewswire/ -- Eisai Co., Ltd. ("Eisai") and Shanghai Henlius Biotech, Inc. ("Henlius") today announced the conclusion of an exclusive commercialization...
► Artikel lesen
DiGHIT 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 Eisai908TOKYO, 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...
► Artikel lesen
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)406STOCKHOLM, 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...
► Artikel lesen
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 Autoinjector291TOKYO (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...
► Artikel lesen
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 Review572If 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...
► Artikel lesen
26.01.FDA Grants Priority Review To Eisai And Biogen's SBLA For LEQEMBI Subcutaneous Autoinjector622WESTON (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...
► Artikel lesen
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 Review1.540If 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...
► Artikel lesen
21.01.Eisai Listed as a Global 100 Most Sustainable Corporation for the Tenth Time317Highest ranked global pharmaceutical companyTOKYO, Jan 21, 2026 - (JCN Newswire) - Eisai Co., Ltd. (Headquarters: Tokyo, CEO: Haruo Naito, "Eisai") announced today that it has been listed in the 2026...
► Artikel lesen
13.01.Eisai and Nuvation Bio Enter into Exclusive Licensing Agreement for Taletrectinib in Europe and Additional Countries Outside the U.S., China and Japan665- Eisai will receive exclusive development, registration and commercialization rights for taletrectinib for the treatment of ROS1-positive non-small cell lung cancer in Europe, the Middle East, Canada...
► Artikel lesen
12.01.Eisai sichert sich Lizenz für Lungenkrebs-Medikament Taletrectinib in Europe und Asien7
07.01.Newron Pharmaceuticals S.p.A.: EA Pharma, a subsidiary of Eisai, Announces the Initiation of its Phase III Clinical Trial with Evenamide, a Novel Treatment for Schizophrenia, in Japan803Newron Pharmaceuticals S.p.A. ("Newron") (SIX: NWRN, XETRA: NP5), a biopharmaceutical company focused on the development of novel therapies for patients with diseases of the central and peripheral...
► Artikel lesen
Weiter >>
133 Nachrichten in den letzten 12 Monaten
Ich würde die Aktie auf Sicht von 6 Monaten
VerkaufenHaltenKaufen
■ Verkaufen
■ Halten
■ Kaufen
1,1,4