Sanofi (SNY)
| Market Cap | 113.67B -17.4% |
| Revenue (ttm) | 54.85B +5.5% |
| Net Income | 9.17B +40.5% |
| EPS | 7.48 +43.6% |
| Shares Out | 1.21B |
| PE Ratio | 12.39 |
| Forward PE | 9.49 |
| Dividend | $1.60 (3.42%) |
| Ex-Dividend Date | May 9, 2025 |
| Volume | 2,227,792 |
| Open | 47.57 |
| Previous Close | 47.08 |
| Day's Range | 46.64 - 47.59 |
| 52-Week Range | 43.32 - 55.73 |
| Beta | 0.32 |
| Analysts | Buy |
| Price Target | 58.00 (+24.04%) |
| Earnings Date | Apr 23, 2026 |
About SNY
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 numbers in EUR Financial StatementsAnalyst Summary
According to 5 analysts, the average rating for SNY stock is "Buy." The 12-month stock price target is $58.0, which is an increase of 24.04% from the latest price.
News
Sanofi (SNY) Gains Authorization for Nuvaxovid in Canada
Sanofi (SNY) Gains Authorization for Nuvaxovid in Canada
Sanofi's Lunsekimig Shows Promise In Respiratory Diseases
(RTTNews) - Sanofi (SNY) announced that its investigational therapy Lunsekimig met both primary and key secondary endpoints in two Phase 2 studies targeting chronic respiratory conditions, underscorin...
From Lungs To Nasal Polyps: Sanofi Finds Success With 2-in-1 Inflammation Blocker
Sanofi SA (NASDAQ: SNY) on Tuesday reported Phase 2 data for its experimental therapy lunsekimig in chronic respiratory diseases, highlighting meaningful improvements in asthma and nasal polyp patien...
Sanofi: Lunsekimig Meets Primary, Key Secondary Endpoints In Phase 2 Respiratory Studies
(RTTNews) - Sanofi (SNY, SAN.PA) said phase 2 studies of lunsekimig in two chronic respiratory diseases met their primary and key secondary endpoints compared to placebo. In both studies, lunsekimig w...
Press Release: Sanofi's lunsekimig met primary and key secondary endpoints in phase 2 respiratory studies in asthma and CRSwNP
Sanofi's lunsekimig met primary and key secondary endpoints in phase 2 respiratory studies in asthma and CRSwNP The AIRCULES phase 2b study achieved its primary and key secondary endpoints in modera...
Press Release: Sanofi's lunsekimig met primary and key secondary endpoints in phase 2 respiratory studies in asthma and CRSwNP
Sanofi's lunsekimig met primary and key secondary endpoints in phase 2 respiratory studies in asthma and CRSwNP The AIRCULES phase 2b study achieved its primary and key secondary endpoints in moderate...
Sanofi Receives EU Conditional Marketing Authorization For Rezurock In Chronic GVHD
(RTTNews) - Sanofi (SNY) has received conditional marketing authorization from the European Commission for Rezurock to treat chronic graft-versus-host disease in adults and in children aged 12 years a...
Sanofi: European Commission Grants Conditional Marketing Authorisation For Rezurock
(RTTNews) - Sanofi (SNY, SAN.PA) said the European Commission has granted a conditional marketing authorisation for Rezurock or belumosudil for the treatment of chronic graft-versus-host disease in ad...
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...
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...
Sanofi Reports Positive Phase 3 Results For Amlitelimab In Atopic Dermatitis
(RTTNews) - Sanofi SA (SNY, SNYNF,SAN.PA) announced encouraging results from three Phase 3 clinical trials—COAST 1, COAST 2, and SHORE—evaluating amlitelimab, a fully human non-T cell depleting monocl...
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
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.
Sanofi: CHMP Adopts Positive Opinion Recommending Approval Of Sarclisa
(RTTNews) - Sanofi (SNY, SAN.PA) announced the European Medicines Agencys Committee for Medicinal Products for Human Use has adopted a positive opinion recommending the approval of Sarclisa or isatuxi...
Sanofi (SNY) Gains Japanese Approval for Dupixent in Treating Bullous Pemphigoid
Sanofi (SNY) Gains Japanese Approval for Dupixent in Treating Bullous Pemphigoid
Sanofi And Regeneron's Dupixent Approved In Japan For Bullous Pemphigoid
(RTTNews) - Sanofi (SNY) and Regeneron Pharmaceuticals (REGN) announced that Japan's Ministry of Health, Labour and Welfare has approved Dupixent (dupilumab) for adults with moderate-to-severe bullous...
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...
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
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 Approval in moderate-to-severe patients was based on pivotal study results show...
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.
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...
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 ...
Sanofi's Venglustat Gets FDA Breakthrough Therapy Designation For Type 3 Gaucher Disease
(RTTNews) - Sanofi (SNY, SAN.PA, SNYNF) announced that the US Food and Drug Administration has granted Breakthrough Therapy designation to Venglustat for the treatment of neurological manifestations o...
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).
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...