Press Releases

06-12 Sanofi’s Tzield approved in the US as the first disease-modifying therapy for patients recently diagnosed with stage 3 type 1 diabetes GL
06-10 Sanofi provides update on MOBILIZE phase 3 study of riliprubart in chronic inflammatory demyelinating polyneuropathy GL
06-08 Sanofi’s Sarclisa subcutaneous approved in the EU as the first anticancer treatment administered via an on-body injector GL
06-04 Sanofi federates the healthcare ecosystem to accelerate the diagnosis of rare diseases in France, Biogen joins accelRare AQ
06-04 Sanofi launches 2026 global employee stock purchase plan GL
06-02 UPC Turns Three: Statistics, Milestones, And Trends AQ
05-29 Sanofi's venglustat accepted for priority review in the US to treat type 3 Gaucher disease AQ
05-28 Sanofi’s venglustat accepted for priority review in the US to treat type 3 Gaucher disease GL
05-18 ATS: phase 2 data demonstrate the superiority of efdoralprin alfa over a standard-of-care augmentation therapy in achieving higher fAAT levels in AATD   GL
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
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