Press Releases

04-29 Annual General Meeting of April 29, 2026 - Belén Garijo appointed as Director and Chief Executive Officer of Sanofi GL
04-27 Sanofi's Cenrifki recommended for EU approval by the CHMP to treat secondary progressive multiple sclerosis without relapses AQ
04-24 Sanofi successfully prices 2.3 billion of bond issue GL
04-24 Sanofi’s Cenrifki (tolebrutinib) recommended for EU approval by the CHMP to treat secondary progressive multiple sclerosis without relapses GL
04-23 Phase 3 EMN24 IsKia Study: Quadruplet Isa-KRd Regimen Significantly Improves MRD Negativity in Newly Diagnosed Multiple Myeloma | DelveInsight's Perspective on Treatment Paradigm Shift AQ
04-23 Q1 2026: double-digit sales and business EPS growth GL
04-22 Sanofi and Regeneron’s Dupixent approved in the US as the first biologic medicine for young children with uncontrolled chronic spontaneous urticaria GL
04-22 Sanofi's Tzield approved in the US to delay the onset of stage 3 type 1 diabetes in young children GL
04-22 Sanofi provides update on the regulatory submission for Sarclisa subcutaneous in the US GL
04-18 ESCMID: Sanofi's Nuvaxovid COVID-19 vaccine showed better tolerability than mNEXSPIKE in head-to-head study GL
04-13 Sanofi and Regeneron’s Dupixent approved in the EU as the first targeted medicine to treat young children with chronic spontaneous urticaria GL
04-08 Sanofi - Combined General Meeting of April 29, 2026 - Availability of Preparatory documents GL
04-07 Sanofi : lunsekimig met primary and key secondary endpoints in phase 2 respiratory studies in asthma and CRSwNP PU
04-07 Sanofi’s lunsekimig met primary and key secondary endpoints in phase 2 respiratory studies in asthma and CRSwNP GL
04-01 Sanofi's Rezurock approved in the EU to treat chronic graft-vs-host disease AQ
03-31 Sanofi’s Rezurock approved in the EU to treat chronic graft-vs-host disease GL
03-30 AAD, new results from Sanofi's amlitelimab phase 3 studies in atopic dermatitis presented in late-breaking research session AQ
03-30 Sanofi's Sarclisa subcutaneous formulation administered via on-body injector recommended for EU approval by the CHMP to treat multiple myeloma AQ
03-28 AAD: new results from Sanofi's amlitelimab phase 3 studies in atopic dermatitis presented in late-breaking research session GL
03-27 Sanofi’s Sarclisa subcutaneous formulation administered via on-body injector recommended for EU approval by the CHMP to treat multiple myeloma GL
03-24 Availability of the Q1 2026 aide-mémoire GL
03-24 Sanofi and Regeneron’s Dupixent approved in Japan as the first targeted medicine to treat adults with bullous pemphigoid GL
03-18 Sanofi’s venglustat earns Breakthrough Therapy designation in the US for type 3 Gaucher disease GL
03-12 Sanofi: Informations relatives au nombre de droits de vote et d'actions - FEVRIER 2026 PU
03-08 Brazil’s EMS buys Medley AQ
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