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WKN: 920657 | ISIN: FR0000120578 | Ticker-Symbol: SNW
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22.04.26 | 15:38
80,90 Euro
-0,10 % -0,08
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LeserMedien
14:59FDA delays decision on Sanofi's subcutaneous Sarclisa4
13:42Sanofi Eyes First On-Body Injector Cancer Therapy As FDA Delays Decision3
12:51Entschlüsselung fehlregulierter Immunreaktionen: Forschung bei Sanofi an neuen Therapieoptionen für Autoimmunerkrankungen305Frankfurt/Main (ots) - Autoimmunerkrankungen betreffen weltweit Millionen von Patient*innen. Sie erfordern oft lebenslange Behandlung. Trotz bedeutender medizinischer Fortschritte sprechen nicht alle...
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09:06Sanofi Says FDA Extends Review Of Sarclisa SC By Up To Three Months398PARIS (dpa-AFX) - Sanofi SA (SNY) on Wednesday said the U.S. Food and Drug Administration has extended by up to three months the timeline to review Sarclisa subcutaneous (SC) formulation in...
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08:36Sanofi Wins FDA Nod To Expand Use Of Type 1 Diabetes Drug In Younger Children284PARIS (dpa-AFX) - Sanofi SA (SNY) on Wednesday said the U.S. Food and Drug Administration has approved Tzield to expand its indication from patients aged eight years and older to those as young...
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07:24FDA expands Sanofi's Tzield use to children as young as 1 for type 1 diabetes delay6
07:22FDA erweitert Zulassung für Sanofis Diabetes-Medikament Tzield auf Kleinkinder15
07:18FDA approves Sanofi's Tzield for children as young as one year5
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07:10Sanofi: Sanofi provides update on the regulatory submission for Sarclisa subcutaneous in the US255Sanofi provides update on the regulatory submission for Sarclisa subcutaneous in the US Paris, April 22, 2026. The US Food and Drug Administration (FDA) has extended by up to three months the target...
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07:10Sanofi: Sanofi's Tzield approved in the US to delay the onset of stage 3 type 1 diabetes in young children244Sanofi's Tzield approved in the US to delay the onset of stage 3 type 1 diabetes in young children Expanded approval includes children aged one year and above with stage 2 T1D to delay the onset...
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MoSanofi touts tolerability of COVID shot Nuvaxovid in head-to-head trial vs. Moderna's mNexspike11
SoSanofi's Nuvaxovid Shows Superior Tolerability Over Moderna's MNEXSPIKE In COMPARE Study742PARIS (dpa-AFX) - Sanofi's (SNY, SNYNF,SAN.PA) protein-based COVID-19 vaccine, Nuvaxovid (NVX-CoV2705), demonstrated a significantly better tolerability profile compared to Moderna's latest...
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SaSanofi: ESCMID: Sanofi's Nuvaxovid COVID-19 vaccine showed better tolerability than mNEXSPIKE in head-to-head study832ESCMID: Sanofi's Nuvaxovid COVID-19 vaccine showed better tolerability than mNEXSPIKE in head-to-head study First head-to-head, double-blind, randomized phase 4 study powered to directly compare the...
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DoDKSH erhält Aufträge von Yeastup und Sanofi18
15.04.Sanofi - 6-K, Report of foreign issuer13
14.04.Sanofi: Information concerning the total number of voting rights and shares - March 20263
13.04.Regeneron und Sanofi bekommen Dupixent-Zulassung für Kinder mit CSU553DJ Regeneron und Sanofi bekommen Dupixent-Zulassung für Kinder mit CSU Von Colin Kellaher DOW JONES--Regeneron Pharmaceuticals und Sanofi haben für ihren Blockbuster-Entzündungshemmer Dupixent...
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13.04.Regeneron, Sanofi Secure EU Nod To Expand Dupixent Use In Young Children With CSU358PARIS (dpa-AFX) - Regeneron Pharmaceuticals, Inc. (REGN) and Sanofi SA (SNY) on Monday said the European Commission has approved Dupixent for treating moderate-to-severe chronic spontaneous...
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13.04.Sanofi, Regeneron's Dupixent approved in EU for young children with chronic urticaria5
13.04.Sanofi: Sanofi and Regeneron's Dupixent approved in the EU as the first targeted medicine to treat young children with chronic spontaneous urticaria557Sanofi and Regeneron's Dupixent approved in the EU as the first targeted medicine to treat young children with chronic spontaneous urticaria Approval in CSU for children two to 11 years of age is...
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