PRESS RELEASE published on 11/25/2025 at 07:00, 10 months 8 days ago Press Release: Sanofi and Regeneron’s Dupixent approved as the first targeted medicine in the EU in over a decade for chronic spontaneous urticaria Sanofi and Regeneron receive EU approval for Dupixent as targeted medicine for chronic spontaneous urticaria, significantly reducing itch and hives compared to placebo Sanofi Dupixent EU Approval Regeneron Chronic Spontaneous Urticaria
PRESS RELEASE published on 11/17/2025 at 18:15, 10 months 16 days ago Sanofi: Disclosure of trading in own shares
BRIEF published on 11/14/2025 at 12:35, 10 months 19 days ago Green light for Sanofi's Teizeild in type 1 diabetes Sanofi Type 1 Diabetes Teizeild CHAMP TN-10 Study
PRESS RELEASE published on 11/14/2025 at 12:30, 10 months 19 days ago Press Release: Sanofi’s Teizeild recommended for EU approval by the CHMP for patients with stage 2 type 1 diabetes Sanofi's Teizeild recommended for EU approval for stage 2 type 1 diabetes based on positive CHMP opinion. TN-10 study shows Teizeild delays the onset of stage 3 T1D Sanofi CHMP EU Approval Type 1 Diabetes Teizeild
BRIEF published on 11/07/2025 at 14:05, 10 months 26 days ago Sanofi and Regeneron's Dupixent: Advances against allergic fungal rhinosinusitis FDA Sanofi Dupixent Regeneron AFRS
PRESS RELEASE published on 11/07/2025 at 14:00, 10 months 26 days ago Press Release: ACAAI: Sanofi and Regeneron’s Dupixent pivotal study met all primary and secondary endpoints, reducing signs and symptoms of allergic fungal rhinosinusitis; sBLA accepted for FDA priority review Sanofi and Regeneron announce positive results from Dupixent pivotal study in allergic fungal rhinosinusitis, with sBLA accepted for FDA priority review FDA Sanofi Dupixent Regeneron AFRS
PRESS RELEASE published on 10/24/2025 at 07:30, 11 months 10 days ago Press release: Q3: continued sales and earnings progress
BRIEF published on 10/20/2025 at 13:35, 11 months 14 days ago Sanofi's Tzield: FDA Fast-Tracks Review for Type 1 Diabetes FDA Sanofi Type 1 Diabetes Expedited Review Tzield
PRESS RELEASE published on 10/20/2025 at 13:30, 11 months 14 days ago Press Release: Sanofi’s Tzield accepted for expedited review in the US for stage 3 type 1 diabetes through FDA Commissioner's National Priority Voucher pilot program Sanofi's Tzield accepted for expedited review by FDA under National Priority Voucher pilot program to delay progression of stage 3 type 1 diabetes. Breakthrough therapy with significant unmet medical need addressed FDA Sanofi Type 1 Diabetes Tzield National Priority Voucher
BRIEF published on 10/20/2025 at 08:35, 11 months 14 days ago Sanofi's AlphaMedix Shows Promise in Treating GEP-NETs Phase 2 Study Sanofi AlphaMedix GEP-NETs Targeted Alpha Therapy
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