Sanofi (LON:0O59)
London · Delayed Price · Currency is GBP · Price in EUR | Market Cap | 75.12B -16.1% |
| Revenue (ttm) | 41.35B +4.8% |
| Net Income | 6.60B +19.9% |
| EPS | 5.42 +23.0% |
| Shares Out | n/a |
| PE Ratio | 11.39 |
| Forward PE | 8.42 |
| Dividend | 3.55 (4.69%) |
| Ex-Dividend Date | May 5, 2026 |
| Volume | 4,330,794 |
| Open | 74.00 |
| Previous Close | 74.14 |
| Day's Range | 71.24 - 74.10 |
| 52-Week Range | 70.92 - 93.50 |
| Beta | 0.28 |
| 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 numbers in EUR Financial StatementsNews
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...
Sanofi (SNY) Drives $24.5M Milestone Payment to MacroGenics
Sanofi (SNY) Drives $24.5M Milestone Payment to MacroGenics
MacroGenics to receive $24.5M milestone payment from Sanofi
MacroGenics (MGNX) announced that it will receive a $24.5M regulatory milestone payment from Sanofi (SNY) following the U.S. Food and Drug Administration’s accelerated approval of TZIELD to delay the ...
Sanofi (SNY) Appoints New R&D Chief Amidst Mixed Expectations
Sanofi (SNY) Appoints New R&D Chief Amidst Mixed Expectations
Sanofi appoints Paulo Fontoura as Global Head of R&D
Sanofi (SNY) announced the appointment of Paulo Fontoura, MD, PhD, FAAN, as Executive Vice President, Global Head of Research & Development Pharma, effective September 1. “He will be a member…
Sanofi investors likely to view new R&D head as a positive, says BofA
After Sanofi (SNY) announced a new head of R&D with Paulo Fontoura replacing Houman Ashrafian, BofA analyst Sachin Jain says investors are likely to view Fontoura’s appointment as a positive…
Japan's MHLW Approves Sanofi's Subcutaneous Sarclisa For Multiple Myeloma
(RTTNews) - Sanofi (SNY) announced that the Ministry of Health, Labour, and Welfare, or MHLW, in Japan, has granted clearance for the Sarclisa subcutaneous (SC) formulation in combination with approve...
Press Release: Sanofi appoints Paulo Fontoura as Global Head of R&D
Sanofi a ppoints Paulo Fontoura as Global Head of R&D Paris , June 22 , 2026. Sanofi today announced the appointment of Paulo F o ntoura , MD, PhD, FAAN, as Executi v e Vice President, G...
Sanofi's Sarclisa Subcutaneous Combination Therapy Gets Japan Approval For Multiple Myeloma
(RTTNews) - French drug major Sanofi (SNY, SAN.PA) announced Friday that Sarclisa (isatuximab) subcutaneous (SC) formulation combination therapy has been approved in Japan for patients with multiple m...
Sanofi: Sanofi's Sarclisa subcutaneous formulation approved in Japan for patients with multiple myeloma
Sanofi's Sarclisa subcutaneous formulation approved in Japan for patients with multiple myeloma Approval based on multiple studies, including the pivotal IRAKLIA phase 3 study which demonstrated no...
Press Release: Sanofi's Sarclisa subcutaneous formulation approved in Japan for patients with multiple myeloma
Sanofi's Sarclisa subcutaneous formulation approved in Japan for patients with multiple myeloma Approval based on multiple studies, including the pivotal IRAKLIA phase 3 study which demonstrated non-i...
Sanofi SA (SNY) Stock Down 3.5% -- Now Undervalued? GF Score: 73/100
Sanofi SA (SNY) Stock Down 3.5% -- Now Undervalued? GF Score: 73/100
Sanofi price target lowered to EUR 95 from EUR 100 at Deutsche Bank
Deutsche Bank lowered the firm’s price target on Sanofi (SNY) to EUR 95 from EUR 100 and keeps a Buy rating on the shares.
Sanofi: Information concerning the total number of voting rights and shares – May 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...
Sanofi (SNY) Gains FDA Approval for Expanded Use of Tzield in Type 1 Diabetes
Sanofi (SNY) Gains FDA Approval for Expanded Use of Tzield in Type 1 Diabetes
FDA Grants Accelerated Approval To Sanofi's Tzield For Children With Stage 3 Type 1 Diabetes
(RTTNews) - Sanofi (SNY) announced that the U.S. Food and Drug Administration has granted accelerated approval to Tzield (teplizumab-mzwv) for delaying the decline in endogenous insulin production in ...
Sanofi: Sanofi's Tzield approved in the US as the first disease-modifying therapy for patients recently diagnosed with stage 3 type 1 diabetes
Sanofi's Tzield approved in the US as the first disease-modifying therapy for patients recently diagnosed with stage 3 type 1 diabetes Accelerated approval in children aged eight to 17 years old re...
FDA approves Sanofi's drug for stage 3 type 1 diabetes in children
The U.S. Food and Drug Administration approved Sanofi's injection to slow the loss of the body's own insulin production in children aged 8 to 17 years recently diagnosed with stage 3 typ...
Strong Buy Rating on Sanofi (SNY) Following Positive Study Results
Strong Buy Rating on Sanofi (SNY) Following Positive Study Results
Wayrilz (rilzabrutinib, Sanofi) Positioned to Define Third-Line Treatment in Warm Autoimmune Hemolytic Anemia (w-AIHA) as IMAAVY (niopcalimab, Jonhson & Johnson) Follows Closely with Positive Data Announcement at EHA 2026
New Spherix Global Insights research finds no clear standard of care beyond second line, creating an opportunity for novel therapies to establish themselves in refractory disease and potentially move ...
Sanofi (SNY) Halts Study, Analyst Says Dianthus Selloff Overstated
Sanofi (SNY) Halts Study, Analyst Says Dianthus Selloff Overstated