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WKN: 662283 | ISIN: US80105N1054 | Ticker-Symbol: SNW2
Siehe auch SANOFI SA
Tradegate
24.06.25 | 10:24
42,200 Euro
+2,93 % +1,200
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NASDAQ Biotech
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MiNovavax Sees Sanofi Vaccine Pact as Model for Future Deals, Some Going Beyond Infectious Disease29
MiKymera adds Gilead as research partner, while advancing new candidate with Sanofi5
MiKymera suffers Sanofi setback but secures $750M Gilead deal7
MiKymera-Aktie fällt - Sanofi IRAK4-Degrader zugunsten eines Kandidaten der nächsten Generation aufgibt16
MiKymera stock falls as Sanofi drops IRAK4 degrader for next-gen candidate11
SANOFI SA ADR Aktie jetzt für 0€ handeln
MiSanofi's Experimental Transplant Rejection Drug Gets FDA Orphan Tag7
MiSanofi To Advance Kymera's KT-485 Into Clinical Study7
MiKymera signs $750m cancer deal with Gilead as Sanofi opts in5
MiKymera Therapeutics, Inc.: Kymera Therapeutics Announces Sanofi IRAK4 Collaboration Update62Sanofi to advance Kymera's next-generation oral IRAK4 degrader development candidate, KT-485, into clinical testing and will not advance KT-474 In preclinical testing, KT-485 demonstrated increased...
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MiFDA approves Sanofi and Regeneron's Dupixent for bullous pemphigoid8
MiSanofi's Riliprubart Secures U.S. Orphan Drug Status For Solid Organ Transplant Rejection207PARIS (dpa-AFX) - The U.S. Food and Drug Administration has granted orphan drug designation to riliprubart for the investigational treatment of antibody-mediated rejection (AMR) in solid organ...
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MiSanofi: Riliprubart earns orphan drug designation in the US for antibody-mediated rejection in solid organ transplantation331Riliprubart earns orphan drug designation in the US for antibody-mediated rejection in solid organ transplantation Ongoing phase 2 study evaluating riliprubart for the potential prevention and treatment...
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DiSanofi - 6-K, Report of foreign issuer7
MoSanofi signs €545M deal to explore Formation's JAK/SYK inhibitor in new indication22
MoFormation Bio Licenses Gusacitinib to Sanofi16
MoSanofi/Regeneron's Dupixent granted FDA approval for bullous pemphigoid7
MoSanofis stiller Milliarden-Coup - warum ein Nischenmedikament plötzlich im Zentrum steht62
MoSanofi's Sarclisa Recommended For EU Approval To Treat Transplant-eligible Newly Diagnosed MM290PARIS (dpa-AFX) - French drug major Sanofi S.A. (SNYNF,SNY) announced Monday that Sarclisa (isatuximab) has been recommended for European Union approval by the Committee for Medicinal Products...
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MoSanofi: Sarclisa recommended for EU approval by the CHMP to treat transplant-eligible newly diagnosed multiple myeloma278Sarclisa recommended for EU approval by the CHMP to treat transplant-eligible newly diagnosed multiple myeloma Recommendation based on GMMG-HD7 phase 3 study demonstrating that Sarclisa with VRd...
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FrFDA Approves Regeneron Sanofi Treatment For Rare Autoimmune Skin Disorder8
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