SAN.PA Sanofi

P/E 22.935184
Forward P/E 8.199263
Price/Sales 1.8442671
Beta 0.277
Div Yield 0.0553%
Market Cap --

Company Analysis

Latest News

Sanofi Rations Pompe Disease Drugs, Following FDA Manufacturing Warning

Sanofi Rations Pompe Disease Drugs, Following FDA Manufacturing Warning

Sanofi is rationing two Pompe disease medications, causing treatment delays or dosage reductions for patients. The shortage stems from manufacturing issues at...

Sanofi Cuts Three Immunology Drugs, Triggers €952 Million Write-Off

Sanofi Cuts Three Immunology Drugs, Triggers €952 Million Write-Off

Sanofi discontinued three immunology drug development programs as part of its H1 2026 financial report. The company halted work on amlitelimab for atopic...

🔴 Sanofi is trading 9% down today on profit-taking and broader sector weakness

🔴 Sanofi is trading 9% down today on profit-taking and broader sector weakness

Sanofi is trading 9% down today at €72.77 following a sharp pullback from recent gains and continued profit-taking pressure. • The stock fell 4.5% in the...

🔴 Sanofi is trading 4.5% down today on profit-taking after recent gains

Sanofi is trading 4.5% down at €76.34 on profit-taking following a sharp pullback from its recent rebound toward the upper end of its 52-week range. • The...

Sanofi Halts Development of Eczema Drug Amlitelimab

Sanofi Halts Development of Eczema Drug Amlitelimab

Sanofi discontinued clinical development of amlitelimab for moderate-to-severe atopic dermatitis on Friday. The company will not seek global regulatory...

Sanofi Sues Pfizer and Moderna, Claiming Infringement of mRNA Delivery Patents

Sanofi Sues Pfizer and Moderna, Claiming Infringement of mRNA Delivery Patents

Sanofi filed patent infringement lawsuits against Pfizer and Moderna in New Jersey federal court. The French drugmaker claims their COVID-19 vaccines use...

Sanofi Wins FDA Approval for First Wearable Cancer Injector, Diversifying Revenue

Sanofi Wins FDA Approval for First Wearable Cancer Injector, Diversifying Revenue

Sanofi received FDA approval for Sarclisa Escena, a subcutaneous treatment for multiple myeloma. This marks the first anticancer therapy approved for...

Sanofi hit with FDA warning, citing adulterated drugs at Irish plant

Sanofi hit with FDA warning, citing adulterated drugs at Irish plant

The U.S. Food and Drug Administration (FDA) issued a warning letter to Sanofi’s Genzyme Ireland Limited facility in Waterford, Ireland. Inspectors identified...

Sanofi Nexviazyme hits goals in rare Pompe disease trial, eyes 2026 filing

Sanofi Nexviazyme hits goals in rare Pompe disease trial, eyes 2026 filing

Sanofi announced that its drug Nexviazyme met all primary and secondary goals in the Phase 3 Baby-COMET study. The trial treated infantile-onset Pompe disease...

Sanofi Taps Roche Veteran Paulo Fontoura to Lead Global R&D Transformation

Sanofi Taps Roche Veteran Paulo Fontoura to Lead Global R&D Transformation

Sanofi appointed Paulo Fontoura as Executive Vice President and Global Head of Research & Development Pharma. The appointment becomes effective September 1,...

Sanofi Wins EU Approval for Cenrifki, First to Target MS Disability

Sanofi Wins EU Approval for Cenrifki, First to Target MS Disability

The European Commission approved Sanofi's drug Cenrifki (tolebrutinib) for adults with secondary progressive multiple sclerosis (SPMS) without recent relapses....

Sanofi Wins Japan Approval for Sarclisa Injection, Reducing Patient Treatment Burden

Sanofi Wins Japan Approval for Sarclisa Injection, Reducing Patient Treatment Burden

Sanofi received approval from Japan’s Ministry of Health, Labour and Welfare for the subcutaneous formulation of Sarclisa. This isatuximab injection treats...

Sanofi wins FDA approval for Tzield, first Stage 3 pediatric diabetes drug

Sanofi wins FDA approval for Tzield, first Stage 3 pediatric diabetes drug

Sanofi received FDA accelerated approval for Tzield (teplizumab-mzwv). The treatment targets children aged eight to 17 recently diagnosed with stage 3 type 1...

Sanofi Halts Phase 3 Riliprubart Trial, Citing Lack of Efficacy

Sanofi Halts Phase 3 Riliprubart Trial, Citing Lack of Efficacy

Sanofi terminated its Phase 3 MOBILIZE clinical trial for riliprubart, an investigational antibody targeting chronic inflammatory demyelinating polyneuropathy...