PRESS RELEASE published on 04/30/2025 at 13:00, 7 months 5 days ago Press Release: Sanofi and CD&R close Opella transaction, create global consumer healthcare leader Sanofi and CD&R close Opella transaction, creating global consumer healthcare leader. Sanofi's sale of a 50.0% stake to CD&R marks a strategic move with total net cash proceeds of around €10 billion Transaction Sanofi CD&R Consumer Healthcare Opella
BRIEF published on 04/08/2025 at 19:15, 7 months 26 days ago Sanofi: Positive Publication of Tolebrutinib Data in NEJM Multiple Sclerosis Sanofi Phase III NEJM Tolebrutinib
PRESS RELEASE published on 04/08/2025 at 19:10, 7 months 26 days ago Press Release: Tolebrutinib phase 3 data published in NEJM demonstrate benefit on disability progression in multiple sclerosis Tolebrutinib phase 3 study in NEJM shows delayed disability progression in multiple sclerosis. Potential first therapy targeting immunologic drivers. US priority review ongoing Multiple Sclerosis Phase 3 NEJM Tolebrutinib Disability Progression
BRIEF published on 04/03/2025 at 07:05, 8 months 2 days ago Sanofi's rilzabrutinib designated an orphan drug in the United States Sanofi Orphan Drug Rilzabrutinib Hemolytic Anemia IgG4-associated Disease
PRESS RELEASE published on 04/03/2025 at 07:00, 8 months 2 days ago Press Release: Rilzabrutinib granted orphan drug designation in the US for two rare diseases with no approved medicines Rilzabrutinib granted orphan drug designation in the US for warm autoimmune hemolytic anemia and IgG4-related disease, potential use in immune thrombocytopenia. Sanofi's novel BTK inhibitor holds promise for rare diseases Orphan Drug Designation Sanofi Rare Diseases Rilzabrutinib BTK Inhibitor
BRIEF published on 03/28/2025 at 21:12, 8 months 7 days ago FDA Approves Qfitlia for Hemophilia A and B Treatment FDA Approval Clinical Trials Hemophilia Treatment Antithrombin-lowering Qfitlia
PRESS RELEASE published on 03/28/2025 at 21:07, 8 months 7 days ago Press Release: Qfitlia approved as the first therapy in the US to treat hemophilia A or B with or without inhibitors Qfitlia (fitusiran) approved as the first US therapy for hemophilia A or B with or without inhibitors, offering consistent protection with few injections, using unique mechanism to reduce bleeding episodes Fitusiran Hemophilia Qfitlia Antithrombin-lowering Therapy Bleed Protection
BRIEF published on 03/28/2025 at 07:05, 8 months 8 days ago Dupixent Approved in Japan as First Biologic for COPD Japan Dupixent COPD Treatment Sanofi-Aventis Biologic Approval
PRESS RELEASE published on 03/28/2025 at 07:00, 8 months 8 days ago Press Release: Dupixent approved as the first-ever biologic medicine in Japan for patients with COPD Dupixent approved as the first-ever biologic medicine in Japan for COPD patients based on pivotal phase 3 results in adults with elevated eosinophils, marking a new treatment approach for COPD Japan COPD Dupixent Phase 3 Results Biologic Medicine
PRESS RELEASE published on 03/24/2025 at 19:27, 8 months 11 days ago Sanofi: Disclosure of trading in own shares
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Published on 12/05/2025 at 15:10, 1 hour 27 minutes ago Mersen: Number of shares and voting rights as of November 30, 2025
Published on 12/05/2025 at 08:45, 7 hours 53 minutes ago Air Liquide to expand and electrify its oxygen facility in Shaanxi, supporting China’s commitment to decarbonize its industry
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Published on 12/04/2025 at 17:44, 22 hours 53 minutes ago Net profit attributable to owners of the parent up by 63% to €122 million, driven by business resilience and the improvement in Elior's contribution