Sanofi (EPA:SAN)

France flag France · Delayed Price · Currency is EUR
85.79
+0.47 (0.55%)
Nov 21, 2025, 11:15 AM CET
0.55%
Market Cap103.82B
Revenue (ttm)45.93B
Net Income (ttm)9.11B
Shares Out1.22B
EPS (ttm)7.39
PE Ratio16.35
Forward PE10.33
Dividend3.92 (4.59%)
Ex-Dividend DateMay 12, 2025
Volume188,609
Average Volume1,691,828
Open85.25
Previous Close85.32
Day's Range85.12 - 86.01
52-Week Range76.15 - 110.88
Beta0.37
RSI43.77
Earnings DateJan 29, 2026

About Sanofi

Sanofi engages in the research, development, manufacture, and marketing of therapeutic solutions. It provides immunology and inflammation, rare diseases, neurology, oncology, and other medicines and vaccines. It also offers poliomyelitis, pertussis, and haemophilus influenzae type b (Hib) pediatric vaccines; respiratory syncytial virus protection and hexavalent combination vaccines protecting against diphtheria, tetanus, pertussis, polio, Hib, and hepatitis B; influenza, booster, meningitis, and travel and endemic vaccines, that includes hepati... [Read more]

Sector Healthcare
Founded 1994
Employees 82,878
Stock Exchange Euronext Paris
Ticker Symbol SAN
Full Company Profile

Financial Performance

In 2024, Sanofi's revenue was 44.29 billion, an increase of 7.73% compared to the previous year's 41.11 billion. Earnings were 5.56 billion, an increase of 2.96%.

Financial Statements

News

Sanofi (SNY) and Bristol Myers Squibb (BMY) Face Legal Action Over Plavix Marketing

Sanofi (SNY) and Bristol Myers Squibb (BMY) Face Legal Action Over Plavix Marketing

11 hours ago - GuruFocus

Bristol Myers, Sanofi sued by Texas over Plavix

Texas Attorney General Ken Paxton sued Bristol Myers Squibb and Sanofi , accusing the drugmakers of failing to disclose that Plavix, which is used to prevent blood clots, does not work effectively for...

13 hours ago - Reuters

Lifordi Immunotherapeutics Secures Strategic Investment from Sanofi Ventures and Additional Capital from Existing Investors

Burlington, Massachusetts--(Newsfile Corp. - November 18, 2025) - Lifordi Immunotherapeutics, Inc., a clinical-stage biotech company developing antibody-drug conjugates (ADCs) for the treatment of aut...

2 days ago - Newsfile Corp

Lifordi Immunotherapeutics Secures Strategic Investment from Sanofi Ventures and Additional Capital from Existing Investors

BURLINGTON, Mass.--(BUSINESS WIRE)-- #ADCs--Lifordi Immunotherapeutics, Inc., a clinical-stage biotech company developing antibody-drug conjugates (ADCs) for the treatment of autoimmune and inflammato...

2 days ago - Business Wire

SNY Makes Notable Cross Below Critical Moving Average

In trading on Tuesday, shares of Sanofi (Symbol: SNY) crossed below their 200 day moving average of $50.97, changing hands as low as $50.48 per share. Sanofi shares are currently trading off about 2.4...

2 days ago - Nasdaq

Global drugmakers rush to boost US presence as tariff threat looms

Global drugmakers are rushing to boost U.S. manufacturing and inventory as the Trump administration weighs a 100% tariff on imported branded and patented drugs.

2 days ago - Reuters

Sanofi (SNY) Gains EMA Endorsement for Diabetes Drug Teizeild

Sanofi (SNY) Gains EMA Endorsement for Diabetes Drug Teizeild

6 days ago - GuruFocus

Sanofi (SNY) Facility Faces Regulatory Challenges

Sanofi (SNY) Facility Faces Regulatory Challenges

6 days ago - GuruFocus

Sanofi's type 1 diabetes drug recommended for EU approval

The European Medicines Agency's committee has recommended approval of French drugmaker Sanofi's first-of-its-kind drug that delays onset of the insulin-dependent stage 3 of type 1 diabetes, it said on...

6 days ago - Reuters

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 by the CHMP for patients with stage 2 type 1 diabetes Recommendation based on the TN-10 study, demonstrating Teizeild's ability to delay the onset of stag...

6 days ago - GlobeNewsWire

Merck (MRK) and Sanofi Await CDC's Hepatitis B Vaccine Decision

Merck (MRK) and Sanofi Await CDC's Hepatitis B Vaccine Decision

8 days ago - GuruFocus

Metagenomi Reports Third Quarter 2025 Financial Results and Announces Strategic Pipeline Prioritization and Leadership Updates

New MGX-001 preclinical data supports advancement into clinical development; Demonstrated curative FVIII activity in non-human primates Prioritized later-stage preclinical pipeline including wholly-ow...

9 days ago - Benzinga

The Zacks Analyst Blog Accenture, Sanofi and Dell

Zacks spotlights fresh research on Accenture, Sanofi, and Dell Technologies, revealing trends in consulting, pharma, and AI-driven tech growth

10 days ago - Nasdaq

Top Research Reports for Accenture, Sanofi & Dell Technologies

Accenture, Sanofi, and Dell Technologies stand out in today's top analyst research picks, each navigating growth and market pressures in distinct ways.

10 days ago - Nasdaq

Novavax Q3 Earnings & Revenues Beat Estimates, '25 Sales View Raised

NVAX exceeds third-quarter expectations, boosted by a Sanofi milestone payment. It lifts its 2025 sales outlook.

13 days ago - Nasdaq

REGN: Regeneron and Sanofi Report Positive Dupixent Trial Results

REGN: Regeneron and Sanofi Report Positive Dupixent Trial Results

13 days ago - GuruFocus

Sanofi And Regeneron's Dupixent Meets Primary Goal In Phase 3 Allergic Fungal Rhinosinusitis Study

(RTTNews) - Sanofi SA (SNY) on Friday announced that the pivotal LIBERTY-AFRS-AIMS phase 3 study of Dupixent, co-developed with Regeneron Pharmaceuticals Inc. (REGN), for the treatment of individuals ...

13 days ago - Nasdaq

Sanofi (SNY) Shares Encouraging Phase 3 Results for Dupixent in AFRS Patients

Sanofi (SNY) Shares Encouraging Phase 3 Results for Dupixent in AFRS Patients

13 days ago - GuruFocus

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

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 Phase...

13 days ago - Benzinga

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

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

13 days ago - GlobeNewsWire

Novavax Completes Marketing Authorization Transfers For Nuvaxovid To Sanofi

(RTTNews) - Novavax (NVAX) has completed the transfer of the U.S. marketing authorization for its COVID-19 vaccine, Nuvaxovid to Sanofi (SNY), enabling Sanofi to take full responsibility for commercia...

16 days ago - Nasdaq