6-K: Strong Q1 Performance and 2025 Guidance Confirmed
SCHEDULE 13G/A: Others
6-K: Dupixent Approved in the US as the First New Targeted Therapy in over a Decade for Chronic Spontaneous Urticaria
6-K: Sanofi's Respiratory Pipeline Advances with New Data in Asthma and Plans for New Clinical Studies in COPD
6-K: Tolebrutinib Phase 3 Data Published in NEJM Demonstrate Benefit on Disability Progression in Multiple Sclerosis
6-K: Rilzabrutinib Granted Orphan Drug Designation in the US for Two Rare Diseases with No Approved Medicines
6-K: Dupixent Approved as the First-Ever Biologic Medicine in Japan for Patients with COPD and Qfitlia Approved as the First Therapy in the US to Treat Hemophilia A or B with or Without Inhibitors
S-8: Initial registration statement for securities to be offered to employees pursuant to employee benefit plans
6-K: Tolebrutinib Regulatory Submission Accepted for Priority Review in the US for Patients with Multiple Sclerosis and Chlamydia Vaccine Candidate Granted Fast Track Designation by the US FDA
S-8 POS: S-8 POS
6-K: Sanofi to Acquire Dren Bio's Bispecific Myeloid Cell Engager for Deep B-Cell Depletion, Broadening Immunology Pipeline
6-K: Dupixent Late-Breaking Positive Pivotal Data in Bullous Pemphigoid Presented at AAD
6-K: Sanofi Successfully Prices Eur 1.5 Billion of Bond Issue
6-K: New Duvakitug Data Reinforce Best-in-Class Potential in Ulcerative Colitis and Crohn's Disease and Sarclisa Approved in Japan for Patients with Newly Diagnosed Multiple Myeloma
6-K: Dupixent sBLA Accepted for FDA Priority Review for the Targeted Treatment of Bullous Pemphigoid and Sanofi and CD&R Sign Opella Share Purchase Agreement
SCHEDULE 13G/A: Others
13F-HR: Information required of institutional investment managers pursuant to Section 13(f)
IRANNOTICE: IRANNOTICE
20-F: FY2024 Annual Report
6-K: Update on Extraintestinal Pathogenic E. coli Vaccine Phase 3 Clinical Study