PRESS RELEASE published on 01/22/2025 at 07:00, 1 year 5 months ago Press Release: Sarclisa approved in the EU as the first anti-CD38 therapy in combination with standard-of-care VRd to treat transplant-ineligible newly diagnosed multiple myeloma EU approves Sarclisa as first anti-CD38 therapy in combination with VRd for transplant-ineligible NDMM based on positive IMROZ study results. Third indication for Sarclisa in the EU Multiple Myeloma Sarclisa EU Approval VRd Anti-CD38 Therapy
BRIEF published on 01/15/2025 at 18:35, 1 year 5 months ago Sanofi: Status of voting rights and shares in November 2024 Voting Rights Actions Regulated Information Sanofi November 2024
BRIEF published on 12/17/2024 at 13:35, 1 year 6 months ago Sanofi and Teva Announce Promising Phase 2b Results for Duvakitug Ulcerative Colitis Crohn’s Disease Duvakitug Phase 2b Results Sanofi And Teva Partnership
PRESS RELEASE published on 12/17/2024 at 13:30, 1 year 6 months ago Press Release: Duvakitug positive phase 2b results demonstrate best-in-class potential in ulcerative colitis and Crohn’s disease Sanofi and Teva announce positive phase 2b results for duvakitug in ulcerative colitis and Crohn's disease, showing promising potential in IBD. Phase 3 development planned Ulcerative Colitis Sanofi Teva Crohn's Disease Duvakitug
BRIEF published on 12/17/2024 at 07:35, 1 year 6 months ago Sanofi Releases Q4 2024 Aide-mémoire for Financial Modelling Financial Results Investors Sanofi Aide-mémoire Q4 2024
PRESS RELEASE published on 12/17/2024 at 07:30, 1 year 6 months ago Press Release: Availability of the Q4 2024 Aide-mémoire Sanofi announces availability of Q4 2024 Aide-mémoire for financial modelling purposes. Document includes details on exclusivity losses and foreign currency impact. Results to be published on January 30, 2025 Sanofi Q4 2024 Financial Modelling Exclusivity Losses Foreign Currency Impact
BRIEF published on 12/13/2024 at 07:05, 1 year 6 months ago FDA Grants Breakthrough Therapy Status to Tolebrutinib for nrSPMS Sanofi Tolebrutinib HERCULES Study FDA Breakthrough NrSPMS
PRESS RELEASE published on 12/13/2024 at 07:00, 1 year 6 months ago Press Release: Tolebrutinib designated Breakthrough Therapy by the FDA for non-relapsing secondary progressive multiple sclerosis FDA designates tolebrutinib as Breakthrough Therapy for non-relapsing SPMS based on positive HERCULES study results. Sanofi awaits regulatory review for this innovative medicine FDA Tolebrutinib HERCULES Study Breakthrough Therapy SPMS
BRIEF published on 12/11/2024 at 07:05, 1 year 6 months ago Sanofi's two combination vaccines against influenza and COVID-19 receive expedited review COVID-19 Sanofi Flu Combined Vaccines Expedited Review
PRESS RELEASE published on 12/11/2024 at 07:00, 1 year 6 months ago Press Release: Two combination vaccine candidates for prevention of influenza and COVID-19 granted Fast Track designation in the US Sanofi's two combination vaccine candidates targeting influenza and COVID-19 granted Fast Track designation in the US. Candidates combine licensed vaccines to assess safety and immunogenicity in older adults COVID-19 Sanofi Influenza Combination Vaccine Fast Track Designation
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