PRESS RELEASE published on 07/16/2025 at 07:00, 10 months 7 days ago Press Release: Sanofi’s SAR446597 earns fast track designation in the US for geographic atrophy due to age-related macular degeneration Sanofi's SAR446597 receives fast track designation in the US for geographic atrophy due to age-related macular degeneration, aiming to address unmet medical needs with innovative gene therapy Gene Therapy Sanofi Fast Track Designation Geographic Atrophy SAR446597
PRESS RELEASE published on 07/15/2025 at 18:30, 10 months 8 days ago Sanofi: Disclosure of trading in own shares
PRESS RELEASE published on 06/30/2025 at 21:33, 10 months 23 days ago Sanofi: Disclosure of trading in own shares
BRIEF published on 06/30/2025 at 07:35, 10 months 23 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, 10 months 23 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, 10 months 28 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, 10 months 28 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, 11 months 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, 11 months 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, 11 months 3 days ago FDA Approves Dupixent for Bullous Pemphigoid Treatment FDA Approval Dupixent Type 2 Inflammation Bullous Pemphigoid Rare Skin Disease
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Published on 05/22/2026 at 18:05, 1 day 6 hours ago Disclosure of transactions in own shares from May 18 to May 22, 2026
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