Sanofi (EPA:SAN)

France flag France · Delayed Price · Currency is EUR
82.58
-0.29 (-0.35%)
Apr 2, 2026, 5:39 PM CET
Market Cap99.72B -21.5%
Revenue (ttm)46.72B +5.5%
Net Income7.81B +40.5%
EPS6.37 +43.6%
Shares Out1.21B
PE Ratio20.49
Forward PE9.77
Dividend4.12 (4.97%)
Ex-Dividend DateMay 5, 2026
Volume1,994,015
Average Volume2,817,628
Open82.10
Previous Close82.87
Day's Range81.90 - 83.04
52-Week Range74.85 - 101.90
Beta0.36
RSI64.72
Earnings DateApr 23, 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 vaccines. It also offers poliomyelitis, pertussis, and haemophilus influenzae type b (Hib) pediatric vaccines; respiratory syncytial virus protection and hexavalent combination vaccines that includes hepatitis A, typhoid, yellow fever, and rabies vaccines. It has a collaboration and license agreement with Exscientia to develop up to 15 novel small-molecule for onc... [Read more]

Sector Healthcare
Founded 1994
Employees 74,846
Stock Exchange Euronext Paris
Ticker Symbol SAN
Full Company Profile

Financial Performance

In 2025, Sanofi's revenue was 46.72 billion, an increase of 5.49% compared to the previous year's 44.29 billion. Earnings were 7.81 billion, an increase of 40.52%.

Financial Statements

News

Press Release: Sanofi's Rezurock approved in the EU to treat chronic graft-vs-host disease

Sanofi's Rezurock approved in the EU to treat chronic graft-vs-host disease Rezurock is now approved in the EU for adults and children aged 12 years and older with chronic GVHD, providing a new medici...

3 days ago - GlobeNewsWire

Press Release: AAD: new results from Sanofi's amlitelimab phase 3 studies in atopic dermatitis presented in late-breaking research session

AAD: new results from Sanofi's amlitelimab phase 3 studies in atopic dermatitis presented in late-breaking research session

5 days ago - GlobeNewsWire

EU regulator backs Sanofi's injectable version of blood cancer drug

French drugmaker Sanofi said on Friday the European Medicines Agency has recommended the ​approval of a subcutaneous version of ‌its blood cancer drug administered through an on-body injector.

6 days ago - Reuters

Press release: Availability of the Q1 2026 aide-mémoire

Availability of the Q1 2026 aide-mémoire Paris, France – March 24, 2026. Sanofi announced today the availability of its Q1 2026 aide-mémoire on the "Investors" page of the company's website: First qua...

9 days ago - GlobeNewsWire

Press Release: Sanofi and Regeneron's Dupixent approved in Japan as the first targeted medicine to treat adults with bullous pemphigoid

Sanofi and Regeneron's Dupixent approved in Japan as the first targeted medicine to treat adults with bullous pemphigoid

9 days ago - GlobeNewsWire

Kali Therapeutics signs deal with Sanofi to develop autoimmune treatment

Kali Therapeutics said on Monday it has entered into a licensing agreement with French drugmaker Sanofi to ​develop the privately held firm's experimental treatment for ‌several autoimmune diseases.

10 days ago - Reuters

Sanofi launches innovation and operation centre in China

French drugmaker Sanofi ​launched an ‌innovation and operation centre in ​the southwestern ​Chinese city of ⁠Chengdu on ​Thursday, the company ​said in a statement released on ​its Chinese ​social med...

13 days ago - Reuters

TrumpRx lists many medicines at prices higher than paid in UK

U.S. President Donald Trump pledged to make prescription drugs cheaper for Americans than anywhere in the world, but his TrumpRx.gov website is not delivering across the board lower prices than those ...

15 days ago - Reuters

Mirecule Expands Strategic FSHD Collaboration with Sanofi

GAITHERSBURG, Md.--(BUSINESS WIRE)--Mirecule expands strategic collaboration with Sanofi on advancement of best-in-class ARC treatment of Facioscapulohumeral Muscular Dystrophy (FSHD).

15 days ago - Business Wire

Press Release: Sanofi's venglustat earns Breakthrough Therapy designation in the US for type 3 Gaucher disease

Sanofi's  venglusta t earns Breakthrough Therapy designation in the US for type 3 Gaucher disease Paris, March 18, 2026 . The US Food and Drug Administration (FDA) has granted Breakthrough Therapy des...

15 days ago - GlobeNewsWire

Big drugmakers must face US overcharge claims on medications for low-income patients

A U.S. appeals court on ​Tuesday revived a whistleblower lawsuit accusing four large drugmakers of ‌defrauding the federal and state governments out of hundreds of millions of dollars by overcharging ...

16 days ago - Reuters

The Big 3: PR, ELF, SNY

From oil, beauty, and therapeutic resource stocks, ‪@ElliottWaveTrader‬'s Tammy Marshall turns to three companies she sees as unsung market opportunities. The Fibonacci Princess offers insight and exa...

16 days ago - Schwab Network

Sanofi: An Undervalued Stock For Long-Term Dividend Growth Investors

Sanofi has increased its dividend for 31 consecutive years. That's a fantastic track record. Sanofi increased its revenue from €34.7 billion in FY 2016 to €43.6 billion in FY 2025. That's a compound a...

17 days ago - Seeking Alpha

Sanofi: Information concerning the total number of voting rights and shares - February 2026

Information concerning the total number of voting rights and shares, provided pursuant to article L. 233-8 II of the Code de commerce (the French Commercial Code) and article 223-16 of the Règlement g...

21 days ago - GlobeNewsWire

Brazil drugmaker EMS eyes overseas deals after buying Sanofi unit

Brazilian drugmaker EMS is open to fresh acquisitions to expand internationally after inking a major deal to buy Sanofi's Brazil-based ​generic drugmaker Medley, and is gearing up to launch its own se...

23 days ago - Reuters

Need Growing EPS And Dividends? Prescribe Sanofi

Sanofi is deeply undervalued, trading at a 29% discount to a $65 fair value estimate, with a forward P/E of 9.2 versus a 10-year average of 13. Robust growth is driven by blockbuster drugs like Dupixe...

27 days ago - Seeking Alpha

Press Release:  Sanofi's Board of Directors proposes the appointment of Christel Heydemann as an independent director

Sanofi's Board of Directors proposes the appointment of Christel  Heydemann  as an independent director

4 weeks ago - GlobeNewsWire

Press Release: Filing of an amendment to the French “Document d'Enregistrement Universel” containing the Annual Financial Report

Filing of an amendment to the French “Document d'Enregistrement Universel” containing the Annual Financial Report Paris, March 4, 2026. Sanofi announces today the filing of an amendment to its “Docume...

4 weeks ago - GlobeNewsWire

Sino Biopharm unit licenses blood cancer drug to Sanofi for up to $1.53 bln

Hong Kong-listed Sino Biopharmaceutical said on Wednesday its unit has ​signed an exclusive global licensing deal ‌with French drugmaker Sanofi worth up to $1.53 billion, giving the European pharma gi...

4 weeks ago - Reuters

Press Release: Sanofi's rilzabrutinib earns orphan drug designation in Japan for IgG4-related disease

Sanofi's rilzabrutinib earns orphan drug designation in Japan for IgG4-related disease Designation based on positive data from a phase 2 study of rilzabrutinib in IgG4-RD Third global orphan drug desi...

4 weeks ago - GlobeNewsWire

Press Release: Sanofi and Regeneron's Dupixent recommended for EU approval to treat chronic spontaneous urticaria in young children with ongoing symptoms despite treatment

Sanofi and Regeneron's Dupixent recommended for EU approval to treat chronic spontaneous urticaria in young children with ongoing symptoms despite treatment

4 weeks ago - GlobeNewsWire

Press Release: Acoziborole Winthrop, developed by DNDi and Sanofi, receives CHMP positive opinion as three-tablet, single-dose treatment for most common form of sleeping sickness

Acoziborole Winthrop, developed by DNDi and Sanofi, receives CHMP positive opinion as three-tablet, single-dose treatment for most common form of sleeping sickness  Recommendation based on phase 2/3 s...

4 weeks ago - GlobeNewsWire

Regeneron, Sanofi Blockbuster Dupixent Scores FDA Nod For Rare Sinus Condition

• Regeneron Pharmaceuticals stock is facing resistance. Why are REGN shares declining?

5 weeks ago - Benzinga

Press Release: Sanofi and Regeneron's Dupixent approved in the US as the first and only medicine for allergic fungal rhinosinusitis

Sanofi and Regeneron's Dupixent approved in the US as the first and only medicine for allergic fungal rhinosinusitis Approval in adults and children aged 6 years and older supported by phase 3 study d...

5 weeks ago - GlobeNewsWire

Texas sues Sanofi for allegedly 'bribing' providers to boost drug prescriptions

Texas Attorney General Ken Paxton on Thursday sued Sanofi for allegedly "bribing" providers to prescribe its medications over alternatives.

6 weeks ago - Reuters