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 | 9.48 |
| Dividend | $1.60 (3.46%) |
| Ex-Dividend Date | May 9, 2025 |
| Volume | 411,704 |
| Open | 46.35 |
| Previous Close | 46.76 |
| Day's Range | 46.06 - 46.47 |
| 52-Week Range | 43.32 - 55.73 |
| Beta | 0.32 |
| Analysts | Buy |
| Price Target | 58.00 (+25.2%) |
| 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 25.20% from the latest price.
News
Sanofi (SNY) Gains EU Approval for Dupixent in Young Patients with CSU
Sanofi (SNY) Gains EU Approval for Dupixent in Young Patients with CSU
Regeneron And Sanofi's Dupixent Gets EC Approval To Treat Children Aged 2-11 Years With CSU
(RTTNews) - Regeneron Pharmaceuticals, Inc. (REGN) and Sanofi announced that the European Commission or EC has approved Dupixent or Dupilumab for the treatment of moderate-to-severe chronic spontaneou...
Sanofi (SNY) and Regeneron (REGN) Gain EU Approval for Dupixent in Young Children
Sanofi (SNY) and Regeneron (REGN) Gain EU Approval for Dupixent in Young Children
Regeneron, Sanofi Secure EU Nod To Expand Dupixent Use In Young Children With CSU
(RTTNews) - Regeneron Pharmaceuticals, Inc. (REGN) and Sanofi SA (SNY) on Monday said the European Commission has approved Dupixent for treating moderate-to-severe chronic spontaneous urticaria (CSU) ...
Press Release: Sanofi and Regeneron's Dupixent approved in the EU as the first targeted medicine to treat young children with chronic spontaneous urticaria
Sanofi and Regeneron's Dupixent approved in the EU as the first targeted medicine to treat young children with chronic spontaneous urticaria
Press Release: Sanofi and Regeneron's Dupixent approved in the EU as the first targeted medicine to treat young children with chronic spontaneous urticaria
Sanofi and Regeneron's Dupixent approved in the EU as the first targeted medicine to treat young children with chronic spontaneous urticaria Approval in CSU for children two to 11 years of age is base...
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...
ACOFP: American College of Osteopathic Family Physicians Convenes Experts for Disease Prevention Summit
CHICAGO, IL / ACCESS Newswire / April 6, 2026 / On April 15, ACOFP, in collaboration with sponsors Sanofi and Merck, will gather 25 osteopathic family physicians in Orlando, Florida, for a focused ...
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...
Sanofi: 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 med...
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...
Sanofi: 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 Across the COAST 1, COAST 2, and SHORE phase 3 studies, amlitelimab, dos...
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: Sanofi's Sarclisa subcutaneous formulation administered via on-body injector recommended for EU approval by the CHMP to treat multiple myeloma
Sanofi's Sarclisa subcutaneous formulation administered via on-body injector recommended for EU approval by the CHMP to treat multiple myeloma Recommendation based on positive results demonstrating...
Sanofi (SNY) Gains Japanese Approval for Dupixent in Treating Bullous Pemphigoid
Sanofi (SNY) Gains Japanese Approval for Dupixent in Treating Bullous Pemphigoid