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Sanofi SA

46.76

-0.3200-0.68%

Post-market: 46.760.00000.00%17:05 EDT

Volume:2.23M

Turnover:104.76M

Market Cap:112.50B

PE:12.44

High:47.59

Open:47.57

Low:46.64

Close:47.08

52wk High:55.73

52wk Low:43.32

Shares:2.41B

Float Shares:2.20B

Volume Ratio:0.88

T/O Rate:0.10%

Dividend:2.27

Dividend Rate:4.86%

EPS(TTM):3.76

EPS(LYR):3.76

ROE:6.66%

ROA:4.65%

PB:1.34

PE(LYR):12.44

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Overview Company News Filings

Dupixent® (dupilumab) Approved in Japan for Children Aged 6 to 11 Years with Bronchial Asthma

Merck (MRK.US), Bristol-Myers Squibb (BMY.US), and Other Pharma Giants Agree to Lower U.S. Drug Prices in Exchange for Tariff Exemptions and Policy Support

Sanofi Reports Deal with US Government to Lower Medicine Costs

MT Newswires Live

Trump Reportedly Strikes Drug Price Deals With 9 Pharma Companies

MT Newswires Live

Deals Are With Amgen, Bristol Myers Squibb, Roche’s Genentech, Gilead, GSK, Merck, Novartis, Sanofi and Boehringer Ingelheim -U.S. Official

THOMSON REUTERS

at Least Seven Drug Companies Are Set to Announce Price Cuts With Trump at White House on Friday, Including Glaxosmithkline, Merck and Sanofi - Wapo

THOMSON REUTERS

Sanofi Needs to Show Progress on Pipeline to Rebuild Investor Trust -- Market Talk

Sanofi SA (SNY.US) Announces Approval of Second-Generation Cardiac Myosin Inhibitor in China

Sanofi Says Efdoralprin Alfa Gets Orphan Drug Designation in EU

MT Newswires Live

Koru Medical Systems Names Eric Schiller as CTO

MT Newswires Live

Sanofi, Dren Bio Collaborate on Next-Gen B-Cell Therapy for Autoimmune Diseases

MT Newswires Live

Sanofi's Multiple Sclerosis Drug Faces Trial And Regulatory Setbacks

Benzinga_recent_news

Sanofi Says Primary Progressive Multiple Sclerosis Drug did not Meet Main Goal in a Phase 3 Trial

MT Newswires Live

Stocks to Watch Monday: iRobot, EchoStar, Rocket Lab, Alibaba -- WSJ

Sanofi’s MS Drug Takes Double Hit With FDA Delay, Trial Failure

Tiger Newspress

Sanofi Says China Approved 2 Rare Blood Disorder Therapies

MT Newswires Live

Dow Jones Top Company Headlines at 3 AM ET: Sanofi's Bleeding-Disorder Treatments Get Approval in China | Broadcom ...

EXCLUSIVE-US FDA launches fresh safety scrutiny of approved RSV therapies for infants

Exclusive-U.S. FDA Officials Inform Merck, Sanofi and AstraZeneca Rsv Antibody Therapies Would Receive Fresh Safety Scrutiny -Sources Familiar With the Situation

THOMSON REUTERS

European Equities Traded in the US as ADRs Little Changed in Monday Trading

MT Newswires Live

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Needs to Show Progress on Pipeline to Rebuild Investor Trust -- Market Talk","url":"https://stock-news.laohu8.com/highlight/detail?id=2592555841","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2592555841?lang=en_us&edition=fundamental","pubTime":"2025-12-19 14:52","pubTimestamp":1766127120,"startTime":"0","endTime":"0","summary":"0652 GMT - Sanofi needs to show signs of pipeline progress after recent setbacks to regain investors' trust and for its shares to recover meaningfully, Berenberg analysts say in a research note. A trial failure and a delay to FDA approval for multiple sclerosis drug candidate tolebrutinib hit shares in the French pharmaceutical company, leaving them at the bottom end of their five-year trading range, according to Berenberg. \"Sanofi continues to trade significantly below the value of marketed assets, offering the deepest discount in large pharma and implying a significant R&D discount,\" the analysts say. \"We view this as overly negative given the pockets of success this year.\" The FDA decision on tolebrutinib as well as clinical-trial results for drug candidates amlitelimab, lunsekimig and duvakitug will be key for Sanofi next year, Berenberg says. ","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://dowjonesnews.com/newdjn/logon.aspx?AL=N","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":null,"symbols":["BK4588","IE00BFXG1179.USD","BK4097","BK4007","SNY","SNYNF","PRGS","BK4585","LU2065732104.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1164213342","title":"Sanofi SA (SNY.US) Announces Approval of Second-Generation Cardiac Myosin Inhibitor in China","url":"https://stock-news.laohu8.com/highlight/detail?id=1164213342","media":"Stock News","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1164213342?lang=en_us&edition=fundamental","pubTime":"2025-12-17 21:16","pubTimestamp":1765977406,"startTime":"0","endTime":"0","summary":"Sanofi SA (SNY.US) announced on December 17 that its second-generation cardiac myosin inhibitor (CMI), Aficamten (brand name: Xin Shu Ping in China), has received approval from the National Medical...","market":"sg","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","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":null,"symbols":["IE00BFXG1179.USD","BK4007","BK4588","BK4585","SNY"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2592952489","title":"Sanofi Says Efdoralprin Alfa Gets Orphan Drug Designation in EU","url":"https://stock-news.laohu8.com/highlight/detail?id=2592952489","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2592952489?lang=en_us&edition=fundamental","pubTime":"2025-12-17 17:54","pubTimestamp":1765965296,"startTime":"0","endTime":"0","summary":"Sanofi  said Wednesday its investigational efdoralprin alfa fusion protein has received the European Medicines Agency's orphan drug designation to potentially treat alpha-1 antitrypsin deficiency-related emphysema, a rare respiratory condition.The decision was based on efdoralprin alfa meeting all primary and secondary endpoints in a global phase 2 trial.Efdoralprin alfa has already received the US Food and Drug Administration's fast track and orphan drug designations, the company said.","market":"us","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":["SNY","BK4007","BK4588","IE00BFXG1179.USD","SNYNF","BK4585","BK4156"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2592841930","title":"Koru Medical Systems Names Eric Schiller as CTO","url":"https://stock-news.laohu8.com/highlight/detail?id=2592841930","media":"MT Newswires Live","labels":["executive"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2592841930?lang=en_us&edition=fundamental","pubTime":"2025-12-17 05:27","pubTimestamp":1765920474,"startTime":"0","endTime":"0","summary":"Koru Medical Systems (KRMD) said late Tuesday that it appointed Eric Schiller as chief technology officer, starting Dec. 29.He previously served as Global Head of device development portfolio at Sanofi (SNY).","market":"nz","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":"executive","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["KRMD","LU1066051225.USD","SNY","IE00BFXG1179.USD","LU1066051811.HKD","CTO","BK4160","LU1066053197.SGD","BK4007","LU1066051498.USD","BK4082","BK4585","BK4588"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2591364402","title":"Sanofi, Dren Bio Collaborate on Next-Gen B-Cell Therapy for Autoimmune Diseases","url":"https://stock-news.laohu8.com/highlight/detail?id=2591364402","media":"MT Newswires Live","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2591364402?lang=en_us&edition=fundamental","pubTime":"2025-12-15 22:18","pubTimestamp":1765808296,"startTime":"0","endTime":"0","summary":"Sanofi  has entered a strategic collaboration with Dren Bio to develop a next-generation B-cell depleting therapy for autoimmune diseases, Dren Bio said on Monday.The company said the agreement builds on Sanofi's recent acquisition of Dren Bio's DR-0201 program, now called SAR448501, which is in phase 1 studies and has shown strong B-cell depletion with potential for sustained treatment-free remission.Under the deal, Dren Bio said it will receive a $100 million upfront payment and could earn up to $1.7 billion in development, regulatory, and commercial milestones.The companies will collaborate on discovery and preclinical work, after which Sanofi will lead development, manufacturing, regulatory, and commercialization, Dren Bio said.Dren Bio has the option to enter a US profit/loss sharing arrangement, co-funding 40% of development costs for US co-promotion rights and a 50/50 split of US profits and losses, the company said.It added that outside the US, Dren Bio remains eligible for mil","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":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["BK4588","SNY","BK4007","IE00BFXG1179.USD","SNYNF","BK4585"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2591644528","title":"Sanofi's Multiple Sclerosis Drug Faces Trial And Regulatory Setbacks","url":"https://stock-news.laohu8.com/highlight/detail?id=2591644528","media":"Benzinga_recent_news","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2591644528?lang=en_us&edition=fundamental","pubTime":"2025-12-15 20:52","pubTimestamp":1765803120,"startTime":"0","endTime":"0","summary":"Sanofi said its Phase 3 PERSEUS trial of tolebrutinib missed the primary endpoint in PPMS, ending plans for regulatory filing.","market":"us","thumbnail":"https://cdn.benzinga.com/files/images/story/2025/12/15/Sanofi-SA.jpeg?optimize=medium&dpr=2&auto=webp&width=120","type":0,"news_type":0,"thumbnails":["https://cdn.benzinga.com/files/images/story/2025/12/15/Sanofi-SA.jpeg?optimize=medium&dpr=2&auto=webp&width=120"],"rights":{"source":"benzinga_recent_news","url":"https://www.benzinga.com/news/fda/25/12/49389528/sanofis-multiple-sclerosis-drug-faces-trial-and-regulatory-setbacks","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.benzinga.com/news/fda/25/12/49389528/sanofis-multiple-sclerosis-drug-faces-trial-and-regulatory-setbacks","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":"benzinga_recent_news","symbols":["SNYNF","BK4007","BK4585","BK4588","SNY","IE00BFXG1179.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2591100046","title":"Sanofi Says Primary Progressive Multiple Sclerosis Drug did not Meet Main Goal in a Phase 3 Trial","url":"https://stock-news.laohu8.com/highlight/detail?id=2591100046","media":"MT Newswires Live","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2591100046?lang=en_us&edition=fundamental","pubTime":"2025-12-15 18:48","pubTimestamp":1765795731,"startTime":"0","endTime":"0","summary":"Sanofi (SNY) said Monday its phase 3 trial of its experimental drug, tolebrutinib, did not meet the main goal of delaying disability progression in patients with primary progressive multiple sclerosis","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":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["LU0731783048.USD","IE00BFSS7M15.SGD","LU0175139822.USD","SG9999004303.SGD","IE0004445239.USD","IE0004445015.USD","LU0170899867.USD","BK4007","LU0208291251.USD","LU1585245621.USD","IE00BZ1G4Q59.USD","IE00B775H168.HKD","BK4107","LU1481011671.HKD","LU0742537680.HKD","LU1069347547.HKD","LU1366192091.USD","BK4533","IE00BN29S564.USD","LU0353189680.USD","LU1983260115.SGD","IE0005OL40V9.USD","LU1235295455.SGD","LU2355687059.USD","IE00B7KXQ091.USD","LU1481011911.USD","LU0138981039.USD","LU0320765489.SGD","LU0772969993.USD","LU1430594728.SGD","LU1718418525.SGD","IE00BJJMRY28.SGD","LU0731783394.SGD","SGXZ23171101.USD","SG9999003800.SGD","PGR","IE00BFSS8Q28.SGD","IE00B4JS1V06.HKD","SNY","BK4588","IE00BKVL7J92.USD","BK4585","LU2087625088.SGD","SNYNF","IE00BFXG1179.USD","LU0354030511.USD","LU1035773651.USD","LU0070302665.USD","IE00BJJMRX11.SGD","LU0289960550.SGD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2591161244","title":"Stocks to Watch Monday: iRobot, EchoStar, Rocket Lab, Alibaba -- WSJ","url":"https://stock-news.laohu8.com/highlight/detail?id=2591161244","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2591161244?lang=en_us&edition=fundamental","pubTime":"2025-12-15 17:53","pubTimestamp":1765792380,"startTime":"0","endTime":"0","summary":"iRobot : The Roomba maker declared bankruptcy over the weekend. It said customer service and app functionality will continue normally during the restructuring. Shares tumbled more than 80% before the bell.EchoStar : Shares of the company, which supplies wireless spectrum to SpaceX, rose about 4% premarket after SpaceX confirmed a Wall Street Journal report that it is preparing to go public next year. Shares in SpaceX rival Rocket Lab  also rallied.Newmont  and Freeport-McMoRan : Shares of the mining companies rose premarket as gold prices headed for a new record closing high.Alibaba  and Baidu : The Chinese internet companies' American depositary receipts declined premarket, tracking Friday's declines in U.S. technology stocks. Plus, data released Monday showed the Chinese economy is weakening.Sanofi : The pharmaceutical company said that a U.S. regulatory decision on an experimental multiple sclerosis treatment would be delayed again, and that a late-stage trial missed its main goal. 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Analysts Expect Strong Results.The consensus is that Broadcom will report October quarter revenue of $17.5 billion, with adjusted earnings per share of $1.87.Paramount Sends Letter to Warner Bros. Shareholders Saying Its Offer Is 'Superior'. Paramount sent a letter to Warner Bros. shareholders that sets out why the offer it has made to acquire all of Warner Bros. is 'superior' to the Warner Bros. transaction with Netflix.For Trump, the Warner Megadeal Talks Are All About CNN. 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