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Sanofi SA

45.70

-0.1550-0.34%

Volume:1.32M

Turnover:60.25M

Market Cap:109.49B

PE:24.51

High:45.74

Open:45.49

Low:45.32

Close:45.85

52wk High:52.68

52wk Low:40.89

Shares:2.40B

Float Shares:2.16B

Volume Ratio:0.61

T/O Rate:0.06%

Dividend:2.40

Dividend Rate:5.26%

EPS(TTM):1.86

EPS(LYR):3.76

ROE:5.71%

ROA:5.09%

PB:1.36

PE(LYR):12.16

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Overview Company News Filings

AstraZeneca Hits Goal in Lung Disease Where Rivals Missed -- Market Talk

Sanofi SA Stock (SNY) Moved Up by 3.33% on Mar 25: Key Drivers Unveiled

Regeneron, Sanofi get approval for Dupixent to treat bullous pemphigoid in Japan

Dupixent® (dupilumab) Approved in Japan as the First Targeted Medicine to Treat Adults with Bullous Pemphigoid (BP)

Sanofi Advances Early Autoimmune Antibody Program With New Phase 1 Study Update

Sanofi SA Stock (SNY) Moved Up by 3.07% on Mar 19: Key Drivers Unveiled

European Equities Traded in the US as American Depositary Receipts Fall Sharply in Thursday Trading

MT Newswires Live

Sanofi Says US FDA Grants Venglustat Breakthrough Therapy Designation for Type 3 Gaucher Disease

MT Newswires Live

Sanofi, Regeneron's Eczema Drug Might Face Competition From Pfizer -- Market Talk

Teva, Blackstone Life Sciences Enter $400 Million Funding Deal to Advance Duvakitug

MT Newswires Live

Sanofi Says Rilzabrutinib Receives Orphan Drug Status in Japan

MT Newswires Live

Sanofi’s Blueprint Medicines presents data on Ayvakit ay AAAAI

Sanofi Says Acoziborole Winthrop for Sleeping Sickness Received Positive CHMP Opinion

MT Newswires Live

Dupixent® (dupilumab) Recommended for EU Approval to Treat Chronic Spontaneous Urticaria (CSU) in Young Children with Ongoing Symptoms Despite Treatment

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Hits Goal in Lung Disease Where Rivals Missed -- Market Talk","url":"https://stock-news.laohu8.com/highlight/detail?id=2622828324","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2622828324?lang=en_us&edition=fundamental","pubTime":"2026-03-27 18:40","pubTimestamp":1774608000,"startTime":"0","endTime":"0","summary":"1039 GMT - AstraZeneca's tozorakimab drug candidate hit the primary objective in two late-stage clinical studies for chronic obstructive pulmonary disease, a condition for which rival candidates from Roche and Sanofi recently fell short, Bank of America analysts say in a research note. 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Equities Traded in the US as American Depositary Receipts Fall Sharply in Thursday Trading","url":"https://stock-news.laohu8.com/highlight/detail?id=2620244042","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2620244042?lang=en_us&edition=fundamental","pubTime":"2026-03-19 23:25","pubTimestamp":1773933927,"startTime":"0","endTime":"0","summary":"European equities traded in the US as American depositary receipts were down sharply late Thursday morning, as the S&P Europe Select ADR Index dropped 0.5% to 1,711.73.From continental Europe, the gainers were led by petroleum refiner Equinor  and oil and gas company Eni , which climbed 8.5% and 3.2% respectively. They were followed by pharmaceutical company Sanofi  and software firm SAP , which advanced 2.4% and 0.7% respectively.The decliners from continental Europe were led by lender Banco Santander  and biopharmaceutical company Grifols , which dropped 2.8% and 3.1% respectively. They were followed by telecommunications company Nokia  and biotech firm BioNTech , which were down 2% and 1.5% respectively.The gainers from the UK were led by oil and gas company BP  and biopharmaceutical company Amarin , which rose 4.3% and 1.3% respectively. They were followed by biotech company Trinity Biotech  and cruise line operator Carnival , which were up 0.9% and 0.6% respectively.The decliners ","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["AKTX","CUK","GRFS","LU0320765646.SGD","BK4207","BK4521","BNTX","IE00BMPRXR70.SGD","AMRN","IE00BMPRXN33.USD","BK4023","IE00BFXG1179.USD","LU1162221912.USD","LNOK","BP","E","BK4551","BK4020","BK4535","BK4548","SNY","AFG","BK4585","BDRX","BK4117","BK4528","BK4568","LU0162691827.USD","BK4107","BK4547","NCNA","NOK","BK4139","LU0072461881.USD","SAP","BK4613","SLN","EQNR","BK4588","SAN","BK7142","LU1829250122.USD","SAN.AU","BK4082","BPH","BK4007","BK4201","TRIB","BK4142"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2620231361","title":"Sanofi Says US FDA Grants Venglustat Breakthrough Therapy Designation for Type 3 Gaucher Disease","url":"https://stock-news.laohu8.com/highlight/detail?id=2620231361","media":"MT Newswires Live","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2620231361?lang=en_us&edition=fundamental","pubTime":"2026-03-18 17:47","pubTimestamp":1773827232,"startTime":"0","endTime":"0","summary":"Sanofi  said Wednesday the US Food and Drug Administration has granted breakthrough therapy designation for its investigational drug venglustat to treat  neurological manifestations of type 3 Gaucher disease.The company said the designation was based on results from a phase 3 study in which venglustat showed statistically significant improvements in neurological symptoms compared with enzyme replacement therapy imiglucerase.The treatment was generally well tolerated, with no new safety signals observed, Sanofi said.The company said it plans to pursue global regulatory filings for venglustat this year.","market":"sh","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["SNYNF","BK4588","LABU","SNY","BK4007","IE00BFXG1179.USD","BK4585"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2618949667","title":"Sanofi, Regeneron's Eczema Drug Might Face Competition From Pfizer -- Market Talk","url":"https://stock-news.laohu8.com/highlight/detail?id=2618949667","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2618949667?lang=en_us&edition=fundamental","pubTime":"2026-03-11 19:02","pubTimestamp":1773226920,"startTime":"0","endTime":"0","summary":"1102 GMT - Sanofi and Regeneron might face competition in the market for eczema treatments after Pfizer reported data for an experimental medicine that showed potential to be the first meaningful rival to their Dupixent blockbuster drug, Citi analysts say in a research note. In a midstage trial, Pfizer's tilrekimig achieve efficacy for eczema--also known as atopic dermatitis--with potential to be competitive against Dupixent and placebo-like safety, Citi says. Results from a late-stage study could come between 2027 and 2028 and approval a year later, suggesting tilrekimig could hurt Dupixent sales in the final years before its patents expire, the analysts say. Sanofi shares fall 0.3%. Regeneron and Pfizer are down 1.2% and 0.3%, respectively, in U.S. premarket trading. ","market":"sg","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU0823434740.USD","IE0002270589.USD","LU2362540622.SGD","LU0456855351.SGD","BK4599","LU0823416689.USD","LU1917777945.USD","BK4533","SG9999011175.SGD","IE00BBT3K403.USD","LU0109394709.USD","IE00B19Z3581.USD","LU0889565916.HKD","LU1023059063.AUD","LU0053666078.USD","BK4007","LU1894683264.USD","LU2362541513.USD","IE00BFXG1179.USD","SG9999002232.USD","PFE","SNY","SGXZ57979304.SGD","BK4568","LU0321505868.SGD","IE00B19Z3B42.SGD","LU0225771236.USD","BK4581","BK4585","IE00BLSP4452.SGD","LU0234572021.USD","IE00BLSP4239.USD","BK4139","LU0882574055.USD","BK4550","LU0170899867.USD","LU0225284248.USD","LU2237438978.USD","REGN","LU1883839398.USD","SG9999002224.SGD","SG9999013999.USD","LU1057294990.SGD","LU0289739699.SGD","BK4534","LU0868494617.USD","LU0320765992.SGD","LU1066051498.USD","LU2468319806.SGD","SG9999003800.SGD","LU0306806265.USD","LU0114720955.EUR","LU0122379950.USD","LU1066053197.SGD","LU0058720904.USD","IE000M9KFDE8.USD","BK4588","LU1974910355.USD","LU1894683348.USD","LU2362541273.HKD","LU0306807586.USD","LU2023250504.SGD","BK4592","LU0985481810.HKD","LU0321505439.SGD","LU0823434583.USD","SG9999001176.USD","LU2106854487.HKD","SG9999001176.SGD","LU2089984988.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2616770723","title":"Teva, Blackstone Life Sciences Enter $400 Million Funding Deal to Advance Duvakitug","url":"https://stock-news.laohu8.com/highlight/detail?id=2616770723","media":"MT Newswires Live","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2616770723?lang=en_us&edition=fundamental","pubTime":"2026-03-04 06:33","pubTimestamp":1772577181,"startTime":"0","endTime":"0","summary":"Teva Pharmaceutical Industries (TEVA) said late Tuesday that funds managed by Blackstone Life Sciences will provide $400 million over four years to support the clinical development of duvakitug.Duvaki","market":"sh","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["BK4559","SNY","BK4585","LU1983299246.USD","LU2324357040.USD","TEVA","BK4596","BK4557","BK4584","IE00BFXG1179.USD","BK4588","BK4007","BK4566"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2616433691","title":"Sanofi Says Rilzabrutinib Receives Orphan Drug Status in Japan","url":"https://stock-news.laohu8.com/highlight/detail?id=2616433691","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2616433691?lang=en_us&edition=fundamental","pubTime":"2026-03-02 17:36","pubTimestamp":1772444190,"startTime":"0","endTime":"0","summary":"Sanofi  said Monday that Japan's Ministry of Health, Labour and Welfare has granted orphan drug designation to its experimental medicine rilzabrutinib for the treatment of IgG4-related disease.The company said orphan drug status in Japan is given to treatments targeting rare diseases or conditions with significant unmet medical needs.Sanofi said rilzabrutinib was evaluated in a phase 2 trial, where 52 weeks of treatment reduced disease flare-ups and other key disease markers, while lowering patients' need for glucocorticoid therapy.","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["BK4588","SNYNF","IE00BFXG1179.USD","SNY","BK4007","BK4585"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2616327873","title":"Sanofi’s Blueprint Medicines presents data on Ayvakit ay AAAAI","url":"https://stock-news.laohu8.com/highlight/detail?id=2616327873","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2616327873?lang=en_us&edition=fundamental","pubTime":"2026-03-02 00:50","pubTimestamp":1772383858,"startTime":"0","endTime":"0","summary":"Blueprint Medicines, a Sanofi (SNY) company, announced Ayvakit data showing clinically meaningful outcomes and a well-tolerated long-term safety pr...","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/sanofis-blueprint-medicines-presents-data-on-ayvakit-ay-aaaai-thefly-news?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/the-fly/sanofis-blueprint-medicines-presents-data-on-ayvakit-ay-aaaai-thefly-news?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["BK4505","BK4585","SNYNF","IE00BFXG1179.USD","SNY","LU0053671581.USD","BPMC","BK4139","BK4588","BK4007"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2614858487","title":"Sanofi Says Acoziborole Winthrop for Sleeping Sickness Received Positive CHMP Opinion","url":"https://stock-news.laohu8.com/highlight/detail?id=2614858487","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2614858487?lang=en_us&edition=fundamental","pubTime":"2026-02-27 20:09","pubTimestamp":1772194144,"startTime":"0","endTime":"0","summary":"Sanofi  said Friday the European Medicines Agency's Committee for Medicinal Products for Human Use has issued a positive opinion for  Acoziborole Winthrop to treat of both early and advanced-stage gambiense sleeping sickness in patients aged 12 years and older.The recommendation for Acoziborole Winthrop as a three-tablet, single-dose oral treatment, granted under an accelerated assessment procedure intended for countries outside the European Union, is expected to facilitate approval in the Democratic Republic of Congo and lead to an update of the World Health Organization's treatment guidelines for sleeping sickness, Sanofi said.The positive opinion for Acoziborole Winthrop, which was co-developed by the Drugs for Neglected Diseases initiative, was based on a phase 2/3 study showing up to 96% success rates at 18 months across both early and advanced stages of T.b. gambiense, the company said.The company said that it will donate the medicine to the WHO through its philanthropic arm 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Treatment","url":"https://stock-news.laohu8.com/highlight/detail?id=2614858092","media":"GlobeNewswire","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2614858092?lang=en_us&edition=fundamental","pubTime":"2026-02-27 20:00","pubTimestamp":1772193600,"startTime":"0","endTime":"0","summary":"If approved, Dupixent would be the first targeted medicine in the EU indicated for children aged 2 to 11 years with CSU inadequately controlled by standard-of-care antihistamine treatment CSU is a 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