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WKN: 858523 | ISIN: JP3256000005 | Ticker-Symbol: KY4
Stuttgart
08.09.26 | 21:55
13,000 Euro
-0,76 % -0,100
Branche
Pharma
Aktienmarkt
Japan 225
1-Jahres-Chart
KYOWA KIRIN CO LTD Chart 1 Jahr
5-Tage-Chart
KYOWA KIRIN CO LTD 5-Tage-Chart
RealtimeGeldBriefZeit
13,00013,40008.09.
13,00013,50008.09.

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01.09.Kyowa Kirin To Lower Cost Of Medicines For American Patients; U.S. To Defer Section 232 Tariffs349BRUSSELS/FRANKFURT/PARIS (dpa-AFX) - Kyowa Kirin (KY4.F, 4151.T), a Japan-based Global Specialty Pharmaceutical company, announced a voluntary agreement with the U.S. government to improve access...
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01.09.Preisvereinbarung mit US-Regierung treibt Kyowa Kirin Aktie an6
KYOWA KIRIN Aktie jetzt für 0€ handeln
31.08.Kyowa Kirin, Inc.: Kyowa Kirin Announces Agreement with U.S. Administration to Reduce Treatment Costs for Americans565Strengthens Kyowa Kirin's commitment to expanding access to medicinesReinforces investment in U.S. manufacturing and innovation TOKYO and PRINCETON, N.J., Aug. 31, 2026 (GLOBE NEWSWIRE) -- Kyowa...
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03.08.Kyowa Kirin Non-GAAP EPS of ¥103.26, revenue of ¥263.63B; reaffirms FY 2026 outlook3
03.08.Kyowa Kirin H1 Profit Surges On Higher Revenue413TOKYO (dpa-AFX) - Kyowa Kirin Co., Ltd. (KYKOY), a Japanese pharmaceutical company, on Monday reported significantly higher profit for the first half of 2026, driven by growth in revenue, primarily...
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22.07.Kyowa Kirin EMEA's Crysvita approved by EC for infants with XLH3
21.07.Kyowa Kirin: Europäische Kommission genehmigt Crysvita (burosumab) für Säuglinge mit X-chromosomaler Hypophosphatämie in der Europäischen Union428Mit dieser Zulassung wird die zugelassene Indikation für Crysvita auf Säuglinge im Alter von 1 Monat bis 1 Jahr ausgeweitet, was eine frühzeitigere Behandlung einer seltenen, fortschreitenden...
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21.07.Kyowa Kirin: European Commission Approves Crysvita (burosumab) for Infants with X-linked Hypophosphataemia in the European Union485Approval expands the approved indication for Crysvita to include infants from 1 month to 1 year of age, enabling earlier intervention in a rare, progressive disease that can impact skeletal development...
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30.06.Kyowa Kirin: New Analyses Advance Understanding of Long-Term Survival Outcomes with Mogamulizumab in Mycosis Fungoides and Sézary Syndrome594Advanced analytical methods integrating clinical trial and real-world data address key evidence gaps in rare, difficult-to-treat blood cancers Across both studies, mogamulizumab was associated with...
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29.06.Dividendenbekanntmachungen (29.06.2026)15.712 Unternehmen  ISIN-Code  Dividende (Währung)  Dividende (EUR)  AGC INC  JP3112000009  105 JPY  0,5701 EUR  ALTER EGO MEDIA SA  GRS541003000 - 0,03 EUR  AOZORA BANK LTD  JP3711200000  23 JPY  0,1248...
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29.06.Kyowa Kirin: New PROSPER Data Demonstrate Real-World Impact of Mogamulizumab on Symptoms and Health-Related Quality of Life in Mycosis Fungoides and Sézary Syndrome707 Clinically meaningful improvements in skin symptoms reported as early as week 4 and sustained over the 48-week study period Data presented at the 6th World Congress of Cutaneous Lymphomas meeting in...
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23.06.The XLH Network and Kyowa Kirin Launch the XLH Community Guidebook to Help People Navigate Lifelong Journey with XLH2
11.06.Kura Oncology, Inc.: Kura Oncology And Kyowa Kirin Report Encouraging Long-Term Results for Ziftomenib / 7+3 Combination In Newly Diagnosed AML664- 12-month OS rate 94% among NPM1-m AML patients and 71% among KMT2A-r AML patients in single-arm KOMET-007 trial - - 96% CRc in newly diagnosed NPM1-m AML; 90% CRc in newly diagnosed KMT2A-r AML...
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10.06.Kyowa Kirin to Present New Complementary Evidence Further Defining Clinical Utility of Mogamulizumab in Cutaneous T-Cell Lymphoma at 2026 WCCL555New Clinical Data, Patient Reported Outcomes, Real-World Utilization, and Comparative-Effectiveness Models to be Featured in Four Oral and One Poster PresentationPRINCETON, N.J., June 10, 2026 (GLOBE...
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02.06.Kura Oncology und Kyowa Kirin legen vielversprechende Studiendaten zu AML-Medikament vor6
02.06.Kura Oncology, Inc.: Kura Oncology and Kyowa Kirin Announce Publication in Blood of Ziftomenib plus Venetoclax / Azacitidine Combination in Patients with R/R NPM1-m AML4
15.05.Kyowa Kirin secures FDA approval for Crysvita dosing update4
14.05.Kyowa Kirin: FDA Approves New Dosing Option for CRYSVITA (burosumab-twza) in Adults With XLH879Expanded dosing options support individualized treatment for adults with XLH PRINCETON, N.J., May 14, 2026 (GLOBE NEWSWIRE) -- Kyowa Kirin, Inc., a wholly owned subsidiary of Kyowa Kirin Co. Ltd....
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12.05.Kura Oncology, Inc.: Kura Oncology and Kyowa Kirin to Present Updated Frontline Ziftomenib / 7+3 Combination Data at EHA 2026 Congress17
07.05.Kyowa Kirin reports Q1 results3
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