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WKN: A41T8R | ISIN: CA8010MA1047 | Ticker-Symbol: SNW0
Frankfurt
03.03.26 | 15:25
12,800 Euro
+0,79 % +0,100
Branche
Pharma
Aktienmarkt
Sonstige
1-Jahres-Chart
SANOFI SA CDR Chart 1 Jahr
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SANOFI SA CDR 5-Tage-Chart

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12:15Sanofi - 6-K, Report of foreign issuer4
MoSanofi (SNY) and Regeneron's Dupixent Recommended for EU Approval4
MoSanofi receives CHMP recommendation for Dupixent expansion in Europe7
SANOFI SA CDR Aktie jetzt für 0€ handeln
MoSanofi receives CHMP recommendation for Dupixent approval in Europe7
MoSanofi: Rilzabrutinib Granted Orphan Drug Designation In Japan For IgG4-related Disease315PARIS (dpa-AFX) - Sanofi (SNY, SAN.PA) announced the Ministry of Health, Labour and Welfare in Japan has granted orphan drug designation to rilzabrutinib, an oral, reversible covalent Bruton's...
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MoSanofi: Sanofi's rilzabrutinib earns orphan drug designation in Japan for IgG4-related disease455Sanofi's rilzabrutinib earns orphan drug designation in Japan for IgG4-related disease Designation based on positive data from a phase 2 study of rilzabrutinib in IgG4-RDThird global orphan drug...
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FrSanofi, Genentech, Kedrion back star-studded bleeding disorder awareness campaign12
FrRegeneron und Sanofi erhalten Empfehlung für erweiterte Dupixent-Zulassung450DJ Regeneron und Sanofi erhalten Empfehlung für erweiterte Dupixent-Zulassung Von Colin Kellaher DOW JONES--Der Ausschuss für Humanarzneimittel (CHMP) der Europäischen Arzneimittel-Agentur...
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FrRegeneron, Sanofi Receive Positive CHMP Opinion For Dupixent In Pediatric CSU324PARIS (dpa-AFX) - Regeneron Pharmaceuticals, Inc. (REGN) and Sanofi SA (SNY) Friday said the European Medicines Agencys Committee for Medicinal Products for Human Use (CHMP) has issued a positive...
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FrSanofi: Sanofi and Regeneron's Dupixent recommended for EU approval to treat chronic spontaneous urticaria in young children with ongoing symptoms despite treatment613Sanofi and Regeneron's Dupixent recommended for EU approval to treat chronic spontaneous urticaria in young children with ongoing symptoms despite treatment If approved, Dupixent would be the first...
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FrSanofi's Acoziborole Receives Positive CHMP Opinion For Sleeping Sickness Treatment446PARIS (dpa-AFX) - Sanofi SA (SNY) on Friday said the European Medicines Agency's Committee for Medicinal Products for Human Use has issued a positive opinion for Acoziborole Winthrop for the...
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FrSanofi's acoziborole gets EU panel backing for sleeping sickness4
FrSanofi: Acoziborole Winthrop, developed by DNDi and Sanofi, receives CHMP positive opinion as three-tablet, single-dose treatment for most common form of sleeping sickness438Acoziborole Winthrop, developed by DNDi and Sanofi, receives CHMP positive opinion as three-tablet, single-dose treatment for most common form of sleeping sickness Recommendation based on phase...
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DoSanofi Consumer Healthcare India Ltd leads gainers in 'A' group20
DoStock Alert: Lupin, Zydus Life, Shaily Engineering, KSB, Sanofi India, KP Energy, RVNL3
MiSanofi assists Boston's World Cup plans with play for local engagement6
MiFDA Approves Sanofi And Regeneron's Dupixent As First Medicine For Allergic Fungal Rhinosinusitis458PARIS (dpa-AFX) - Sanofi (SNY, SAN.PA) said FDA has approved Dupixent or dupilumab for the treatment of adult and pediatric patients aged 6 years and older with allergic fungal rhinosinusitis...
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24.02.Regeneron, Sanofi Blockbuster Dupixent Scores FDA Nod For Rare Sinus Condition13
24.02.Regeneron, Sanofi win Dupixent label expansion for allergic fungal rhinosinusitis5
24.02.Sanofi: Sanofi and Regeneron's Dupixent approved in the US as the first and only medicine for allergic fungal rhinosinusitis1.917Sanofi and Regeneron's Dupixent approved in the US as the first and only medicine for allergic fungal rhinosinusitis Approval in adults and children aged 6 years and older supported by phase 3 study...
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