Sanofi (FRA:SNW2)
Germany · Delayed Price · Currency is EUR | Market Cap | 92.34B -9.0% |
| Revenue (ttm) | 47.35B +4.8% |
| Net Income | 7.56B +19.9% |
| EPS | 6.20 +23.0% |
| Shares Out | n/a |
| PE Ratio | 12.22 |
| Forward PE | 8.77 |
| Dividend | 1.50 (3.93%) |
| Ex-Dividend Date | May 4, 2026 |
| Volume | n/a |
| Open | 38.00 |
| Previous Close | 37.60 |
| Day's Range | 37.80 - 38.00 |
| 52-Week Range | 35.60 - 45.00 |
| Beta | n/a |
| Analysts | n/a |
| Price Target | n/a |
| Earnings Date | Jul 30, 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]
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 StatementsNews
Sanofi sues Pfizer, Moderna over COVID shot technology
Sanofi has sued Pfizer and Moderna , alleging that their COVID-19 vaccines infringe several of the French pharmaceutical company's patents.
Sanofi (SNY) Secures FDA Approval for Subcutaneous Sarclisa Escena in Multiple Myeloma
Sanofi (SNY) Secures FDA Approval for Subcutaneous Sarclisa Escena in Multiple Myeloma
Sanofi (SNY) Receives FDA Approval for Subcutaneous Sarclisa Escena
Sanofi (SNY) Receives FDA Approval for Subcutaneous Sarclisa Escena
Sanofi Says FDA Approves Sarclisa Escena SC As First Anticancer Treatment Via On-body Injector
(RTTNews) - French drug major Sanofi SA (SNYNF, SNY) announced Friday that the US Food and Drug Administration (FDA) has approved subcutaneous (SC) Sarclisa Escena administered via the CirCLIQ on-body...
Sanofi announces subcutaneous Sarclisa Escena approved in U.S.
The U.S. Food and Drug Administration has approved subcutaneous Sarclisa Escena in combination with standard-of-care regimens for the treatment of patients with multiple myeloma across all existing in...
Press Release: Sanofi's subcutaneous Sarclisa Escena approved in the US as first anticancer treatment administered via on-body injector
Sanofi's subcutaneous Sarclisa Escena approved in the US as first anticancer treatment administered via on-body injector
US FDA approves Sanofi's wearable injector form of blood cancer drug
The U.S. Food and Drug Administration said on Friday it has approved Sanofi's blood cancer drug, Sarclisa, which can be given under the skin through a wearable injector, offering multiple m...
Sanofi price target lowered to $49 from $52 at Morgan Stanley
Morgan Stanley analyst Sarita Kapila lowered the firm’s price target on Sanofi (SNY) to $49 from $52 and keeps an Equal Weight rating on the shares. Sanofi appears set for…
EU seeks feedback on Sanofi's commitments addressing suspected anti-competitive behaviour
The European Commission said on Wednesday it would seek feedback on commitments offered by French pharmaceutical company Sanofi to address concerns that it may have breached competition rules in ...
Sanofi SA (SNY) Shares Surge 3.7% -- What GF Score of 68 Tells Investors
Sanofi SA (SNY) Shares Surge 3.7% -- What GF Score of 68 Tells Investors
Press Release: Availability of the aide-mémoire for Q2 2026 results
Availability of the aide-mémoire for Q2 2026 results Paris, France – July 1, 2026. Sanofi announced today the availability of the aide-mémoire for Q2 2026 results on the "Investors" page of sanofi.com...
Bargain Hunters: These 3 High-Yielding Stocks Recently Hit New 52-Week Lows
When dividend stocks drop in value, investors have the opportunity to secure some higher-than-typical yields. The stocks listed here haven't been doing well this year, but they offer some attractive d...
Sanofi's Nexviazyme Achieves Key Endpoints In Infantile-Onset Pompe Disease Phase 3 Study
(RTTNews) - Sanofi (SNY) announced that Nexviazyme (avalglucosidase alfa) met all primary secondary endpoints in the Baby-COMET Phase 3 trial for infantile-onset Pompe disease. The study showed that t...
Sanofi (SNY) Reports Positive Phase 3 Results for Nexviazyme in Pompe Disease
Sanofi (SNY) Reports Positive Phase 3 Results for Nexviazyme in Pompe Disease
Sanofi Faces EU Probe With Fines Possibly Reaching 10%
Sanofi Faces EU Probe With Fines Possibly Reaching 10%
Sanofi (SNY) Faces EU Antitrust Investigation Over Vaccine Marketing Practices
Sanofi (SNY) Faces EU Antitrust Investigation Over Vaccine Marketing Practices
EU Commission opens antitrust probe into Sanofi's flu vaccine campaign
The European Commission opened on Friday an investigation into whether French drug giant Sanofi breached EU competition rules in a flu vaccine marketing campaign.
Is Kymera Therapeutics The Next Big Rival To Regeneron And Sanofi?
Kymera Therapeutics shares catapulted Thursday after the company wrapped enrollment in an eczema study six months ahead of expectations.
Press Release: Sanofi Foundation opens new chapter centered on future generations
Sanofi Foundation opens new chapter centered on future generations Paris, June 2 5 , 2026 . The Sanofi Foundation is opening a new chapter with a strengthened commitment to children and young people, ...
MacroGenics To Receive $24.5 Mln Milestone Payment From Sanofi For Recent TZIELD Approval
(RTTNews) - MacroGenics, Inc. (MGNX), a clinical-stage biopharmaceutical company, announced that it will receive a $24.5 million regulatory milestone payment from Sanofi following the recently granted...
Sanofi Wins EU Approval For Cenrifki As First Disability-Targeting Therapy For SPMS Without Relapses
(RTTNews) - Sanofi (SNY) announced that the European Commission has approved Cenrifki (tolebrutinib) as the first medicine in the European Union specifically designed to slow disability progression in...
Sanofi Receives Marketing Rights For Wayrilz In Immune Thrombocytopenia From Japan's MHLW
(RTTNews) - Sanofi (SNY) announced that the Ministry of Health, Labour, and Welfare (MHLW) in Japan has granted marketing and manufacturing approval for Wayrilz in the treatment of persistent or chron...
Sanofi Multiple Sclerosis Drug Gets EU Approval
The authorization of Cenrifki for the treatment of secondary progressive multiple sclerosis without relapses follows a rejection from U.S. drug regulators.
Press Release: Sanofi's Wayrilz approved in Japan to treat immune thrombocytopenia
Sanofi's Wayrilz approved in Japan to treat immune thrombocytopenia Wayrilz is a BTK inhibitor that works through multi-immune modulation to help address the underlying causes of immune thrombocytopen...