PRESS RELEASE published on 06/30/2025 at 21:33, 5 months 4 days ago Sanofi: Disclosure of trading in own shares
BRIEF published on 06/30/2025 at 07:35, 5 months 5 days ago Sanofi Releases Q2 2025 Aide Mémoire Forward-looking Statements Investor Information Financial Modeling Aide Mémoire Sanofi Q2 2025
PRESS RELEASE published on 06/30/2025 at 07:30, 5 months 5 days ago Press release: Availability of the Q2 2025 Aide mémoire Sanofi releases Q2 2025 Aide mémoire for financial modelling, to be published on July 31, 2025. Company details its commitment to innovation and impact in healthcare Innovation Sanofi Aide Mémoire Financial Modelling Q2 2025
BRIEF published on 06/25/2025 at 07:05, 5 months 10 days ago Riliprubart Granted Orphan Drug Designation in the United States FDA Immunology Orphan Drug Riliprubart Kidney Transplant
PRESS RELEASE published on 06/25/2025 at 07:00, 5 months 10 days ago Press Release: Riliprubart earns orphan drug designation in the US for antibody-mediated rejection in solid organ transplantation Sanofi's riliprubart granted orphan drug designation by FDA for antibody-mediated rejection in solid organ transplantation, addressing critical unmet need in transplant medicine Orphan Drug Designation Sanofi Riliprubart Antibody-mediated Rejection Solid Organ Transplantation
BRIEF published on 06/23/2025 at 07:05, 5 months 12 days ago Sarclisa Gains EU Recommendation for Multiple Myeloma Treatment Multiple Myeloma Phase 3 Study Sarclisa CHMP Approval Induction Therapy
PRESS RELEASE published on 06/23/2025 at 07:00, 5 months 12 days ago Press Release: Sarclisa recommended for EU approval by the CHMP to treat transplant-eligible newly diagnosed multiple myeloma Sarclisa recommended for EU approval by CHMP for transplant-eligible newly diagnosed multiple myeloma based on GMMG-HD7 study. Potential to improve outcomes in frontline setting globally Multiple Myeloma Sarclisa EU Approval GMMG-HD7 Study CHMP Recommendation
BRIEF published on 06/20/2025 at 07:05, 5 months 15 days ago FDA Approves Dupixent for Bullous Pemphigoid Treatment FDA Approval Dupixent Type 2 Inflammation Bullous Pemphigoid Rare Skin Disease
PRESS RELEASE published on 06/20/2025 at 07:00, 5 months 15 days ago Press Release: Dupixent approved in the US as the only targeted medicine to treat patients with bullous pemphigoid Dupixent approved in the US as the only targeted medicine for bullous pemphigoid, meeting the critical treatment needs of patients with uncontrolled disease FDA Approval Chronic Disease Dupixent Type 2 Inflammation Bullous Pemphigoid
BRIEF published on 06/17/2025 at 13:45, 5 months 18 days ago Sanofi Successfully Prices €1.5 Billion Bond Issue Bond Issue Corporate Financing Sanofi Fixed-rate Notes Euro Medium Term Note
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Published on 12/04/2025 at 17:45, 22 hours 48 minutes ago MONTHLY INFORMATION RELATING TO THE TOTAL NUMBER OF VOTING RIGHTS AND SHARES MAKING UP THE SHARE CAPITAL
Published on 12/04/2025 at 17:44, 22 hours 49 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