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Sanofi SA

45.64

-0.2057-0.45%

Volume:1.05M

Turnover:47.78M

Market Cap:109.36B

PE:24.48

High:45.70

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:0.65

T/O Rate:0.05%

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):12.14

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Overview Company News Filings

European Equities Traded in the US as American Depositary Receipts Rise in Wednesday Trading

MT Newswires Live

European Equities Traded in the US as American Depositary Receipts Surge in Monday Trading

MT Newswires Live

Sanofi Says US FDA Approved Tzield for Recently Diagnosed Stage 3 Type 1 Diabetes in Children

MT Newswires Live

Sanofi's Tzield Receives FDA Approval for Diabetes Treatment

Buy Dianthus on weakness amid ‘overdone’ selloff, says H.C. Wainwright

Exchange-Traded Funds, Equity Futures Lower Pre-Bell Wednesday Amid Renewed US-Iran Clashes

MT Newswires Live

Dianthus sinks after Sanofi halts CIDP Phase 3 study

Sanofi to halt riliprubart Mobilize phase 3 study

Sanofi's Development Pipeline Stumbles Again as Rare Disease Drug Trial Halts, Adding Pressure on New CEO

Sanofi Stops Late-Stage Trial of Autoimmune Disease Therapy After Interim Review

MT Newswires Live

Sanofi to Stop Late-Stage Study of Immune-Disorder Drug

European Equities Traded in the US as American Depositary Receipts Start Week Higher in Monday Trading

MT Newswires Live

Sanofi's Subcutaneous Sarclisa Approved in EU Across Multiple Myeloma Indications

MT Newswires Live

Movement Alert｜Sanofi Rises 4.59% in Regular Trading, First-in-Class Drug Venglustat Granted FDA Priority Review for Rare Disease

Movement Alert｜Sanofi Rises 3.09% in Pre-Market Trading, First-in-Class Drug Venglustat Granted FDA Priority Review

Sanofi's Groundbreaking Drug Venglustat Seeks FDA Approval for Type 3 Gaucher Disease

Sanofi announces FDA grants priority review to venglustat new drug application

Sanofi Granted FDA Priority Review for Potential Treatment of Rare Gaucher Disease

MT Newswires Live

Sanofi reports ElevAATe trial of efdoralprin alfa meets primary endpoint

Regeneron Pharmaceuticals Trial Miss May Raise Broader Strategy Questions, RBC Says

MT Newswires Live

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Equities Traded in the US as American Depositary Receipts Rise in Wednesday Trading","url":"https://stock-news.laohu8.com/highlight/detail?id=2644747343","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2644747343?lang=en_us&edition=fundamental","pubTime":"2026-06-17 23:10","pubTimestamp":1781709044,"startTime":"0","endTime":"0","summary":"European equities traded in the US as American depositary receipts were sharply higher late Wednesday morning, rising 1.28% to 1,926.15 on the S&P Europe Select ADR Index.From continental Europe, the gainers were led by lenders Banco Santander  and Banco Bilbao Vizcaya Argentaria , which advanced 2.5% and 2.3% respectively. They were followed by biopharmaceutical firm argenx  and biotech firm BioNTech , which rose 2.1% and 2% respectively.The decliners from continental Europe were led by pharmaceutical company Sanofi  and telecommunications company Nokia , which dropped 2% and 1.4% respectively. They were followed by software firm SAP  and telecommunications company Ericsson , which were off 1% and 0.8% respectively.The gainers from the UK were led by Mereo BioPharma Group  and lender Barclays , which rose 9% and 3.6% respectively. They were followed by Akari Therapeutics  and Bicycle Therapeutics , which advanced 3.3% and 2.7% respectively.The decliners from the UK and Ireland were le","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":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["AKTX","SHEH","LU1829250122.USD","LU2543165471.USD","BK4547","AFG","SHEL","EPV","BTI","LU0109394709.USD","BK4548","BPH","IE0002141913.USD","BK4075","BK4591","LU0889565916.HKD","BK4132","BTI.AU","BBVA","SAN.AU","BK4020","VOD","MREO","BK4023","ARGX","BK4551","BCYC","BK4515","IE00BJJMRZ35.SGD","BK4107","LNOK","BNTX","LU0300736062.USD","BK4007","BK4613","NOK","IEUR","BK4554","BK4585","BP","IE0009355771.USD","SNY","BCS","SAN","SAP","IE00BFTCPJ56.SGD","BK4568","BK4528","ERIC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2643204182","title":"European Equities Traded in the US as American Depositary Receipts Surge in Monday Trading","url":"https://stock-news.laohu8.com/highlight/detail?id=2643204182","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2643204182?lang=en_us&edition=fundamental","pubTime":"2026-06-15 23:09","pubTimestamp":1781536187,"startTime":"0","endTime":"0","summary":"European equities traded in the US as American depositary receipts started the week significantly higher late Monday morning, climbing 1.83% to 2,900.33 on the S&P Europe Select ADR Index.From continental Europe, the gainers were led by accommodations booking site trivago  and semiconductor company Sequans Communications , which rose 11% and 6.7% respectively. They were followed by internet browser company Opera  and lender Banco Santander , which were up 3.3% and 2.7% respectively.The decliners from continental Europe were led by petroleum refiner Equinor  and oil and gas company Eni , which dropped 5.6% and 4.3% respectively. They were followed by medical device maker EDAP TMS  and pharmaceutical company Sanofi , which were down 1.4% and 0.6%.The gainers from the UK were led by pharmaceutical company Silence Therapeutics  and biopharmaceutical company Akari Therapeutics , which advanced 3.7% and 3% respectively. They were followed by biopharmaceutical companies Mereo BioPharma Group ","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":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["SAN.AU","DBC","BK4201","BPH","BK4007","LU0278409577.USD","SHEH","FTXN","SNY","AKTX","SHEL","SQNS","DIG","PXE","LU0320765646.SGD","TRVG","VDE","BK4132","BK4023","ERX","IEUR","LU1829250122.USD","GUSH","SLN","DRLL","EPV","TRIB","DBE","XES","IEO","AFG","DRIP","FOCL","BDRX","BK4139","VOD","EQNR","IXC","PXJ","LU1162221912.USD","USE","E","WTIU","OPRA","BP","BK4082","LU0072461881.USD","SAN","MREO"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2643427166","title":"Sanofi Says US FDA Approved Tzield for Recently Diagnosed Stage 3 Type 1 Diabetes in Children","url":"https://stock-news.laohu8.com/highlight/detail?id=2643427166","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2643427166?lang=en_us&edition=fundamental","pubTime":"2026-06-15 17:19","pubTimestamp":1781515189,"startTime":"0","endTime":"0","summary":"Sanofi  has received US Food and Drug Administration accelerated approval for Tzield to delay the decline in endogenous insulin production in children aged 8 to 17 years recently diagnosed with stage 3 type 1 diabetes, the company said Friday.The approval was supported by data from a phase 3 study in which Tzield significantly slowed the decline in mean C-peptide levels, compared with placebo, the company said.Adverse events observed in the study were consistent with previous findings, according to the company.","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","LABU","BK4007","SNYNF","BK4588","IE00BFXG1179.USD","BK4585"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2643215430","title":"Sanofi's Tzield Receives FDA Approval for Diabetes Treatment","url":"https://stock-news.laohu8.com/highlight/detail?id=2643215430","media":"Dow Jones","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2643215430?lang=en_us&edition=fundamental","pubTime":"2026-06-13 06:41","pubTimestamp":1781304060,"startTime":"0","endTime":"0","summary":"Sanofi secured accelerated approval from the Food and Drug Administration for its drug Tzield to be used in the treatment of people with the autoimmune and progressive nature of stage 3 type 1 diabetes. The company said Friday that the therapy can delay the decline in endogenous insulin production in children between the ages of eight and 17, who have recently been diagnosed with stage 3 type 1 diabetes.\"Approximately 64,000 people are diagnosed with T1D every year,\" said Aaron Kowalski, chief executive of Breakthrough T1D. \"We are excited that the approval of Tzield in this indication provides a treatment option for certain patients diagnosed in stage 3 T1D, which is when many start experiencing common symptoms of the disease.\". Sanofi said the treatment has previously received approvals in the U.K., European Union, China, Australia, Canada, Israel, Saudi Arabia, the United Arab Emirates, Kuwait, Brazil and Switzerland.Regulatory reviews are ongoing in other jurisdictions around the w","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":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IE00BFXG1179.USD","SNY","BK4585","LABU","BK4588","BK4007","SNYNF"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2642421509","title":"Buy Dianthus on weakness amid ‘overdone’ selloff, says H.C. Wainwright","url":"https://stock-news.laohu8.com/highlight/detail?id=2642421509","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2642421509?lang=en_us&edition=fundamental","pubTime":"2026-06-10 21:40","pubTimestamp":1781098833,"startTime":"0","endTime":"0","summary":"After Sanofi (SNY) announced that it is stopping the pivotal MOBILIZE study evaluating riliprubart in chronic inflammatory demyelinating polyneurop...","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/buy-dianthus-on-weakness-amid-overdone-selloff-says-h-c-wainwright-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/buy-dianthus-on-weakness-amid-overdone-selloff-says-h-c-wainwright-thefly-news?utm_source=itigerup.com&utm_medium=referral","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":"tipranks_highlight","symbols":["SNY","BK4588","BK4585","IE00BFXG1179.USD","BK4007"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2642548429","title":"Exchange-Traded Funds, Equity Futures Lower Pre-Bell Wednesday Amid Renewed US-Iran Clashes","url":"https://stock-news.laohu8.com/highlight/detail?id=2642548429","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2642548429?lang=en_us&edition=fundamental","pubTime":"2026-06-10 21:05","pubTimestamp":1781096737,"startTime":"0","endTime":"0","summary":"The broad market exchange-traded fund SPDR S&P 500 ETF Trust (SPY) was down 1%, and the actively traded Invesco QQQ Trust (QQQ) retreated by 1.6% in Wednesday's premarket activity, amid renewed clashe","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":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["XLY","CNM","XRT","FAZ","RTH","SE","IPK","SOXX","SNY","EEM","IGM","USO","XLK","EQR","EETH","XLP","IYK","RTH.AU","VDC","EXI","XLI","BETH","BX","VIS","VHT.AU","QQQ","VHT","XLE","XLV","IGV","UNG","GLD","FDN","APA","BITO","FAS","SPY.AU","IVV","IBB","APA.AU","IYE","SLV","TSM","IYH","XSD","IYJ","IYW","SPY",".IXIC","XLF"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2642423107","title":"Dianthus sinks after Sanofi halts CIDP Phase 3 study","url":"https://stock-news.laohu8.com/highlight/detail?id=2642423107","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2642423107?lang=en_us&edition=fundamental","pubTime":"2026-06-10 19:33","pubTimestamp":1781091197,"startTime":"0","endTime":"0","summary":"Shares of Dianthus Therapeutics (DNTH) after sinking after Sanofi (SNY) announced that its riliprubart Phase 3 study in patients with chronic infla...","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/dianthus-sinks-after-sanofi-halts-cidp-phase-3-study-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/dianthus-sinks-after-sanofi-halts-cidp-phase-3-study-thefly-news?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-2","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["SNY","BK4007","BK4588","BK4585","IE00BFXG1179.USD","BK4139","DNTH","SNYNF"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2642447774","title":"Sanofi to halt riliprubart Mobilize phase 3 study","url":"https://stock-news.laohu8.com/highlight/detail?id=2642447774","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2642447774?lang=en_us&edition=fundamental","pubTime":"2026-06-10 18:17","pubTimestamp":1781086620,"startTime":"0","endTime":"0","summary":"Sanofi (SNY) announced that the riliprubart Mobilize phase 3 study in patients with chronic inflammatory demyelinating polyneuropathy, CIDP, refrac...","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/sanofi-to-halt-riliprubart-mobilize-phase-3-study-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/sanofi-to-halt-riliprubart-mobilize-phase-3-study-thefly-news?utm_source=itigerup.com&utm_medium=referral","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":"tipranks_highlight","symbols":["IE00BFXG1179.USD","SNY","BK4585","SNYNF","BK4588","BK4007"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1172294096","title":"Sanofi's Development Pipeline Stumbles Again as Rare Disease Drug Trial Halts, Adding Pressure on New CEO","url":"https://stock-news.laohu8.com/highlight/detail?id=1172294096","media":"Stock News","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1172294096?lang=en_us&edition=fundamental","pubTime":"2026-06-10 16:18","pubTimestamp":1781079513,"startTime":"0","endTime":"0","summary":"The French pharmaceutical giant Sanofi SA (SNY.US) announced on Wednesday that it is ending a late-stage clinical trial early for an experimental drug targeting a rare autoimmune disease, as the...","market":"sg","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-2","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IE00BFXG1179.USD","III","BK4588","BK4134","BK4007","SNY","BK4585"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2642114446","title":"Sanofi Stops Late-Stage Trial of Autoimmune Disease Therapy After Interim Review","url":"https://stock-news.laohu8.com/highlight/detail?id=2642114446","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2642114446?lang=en_us&edition=fundamental","pubTime":"2026-06-10 16:08","pubTimestamp":1781078933,"startTime":"0","endTime":"0","summary":"Sanofi (SNY) said Wednesday that it will discontinue a phase 3 trial of its experimental drug riliprubart in patients with a type of chronic inflammatory demyelinating polyneuropathy after an interim ","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":["SNYNF","BK4007","SNY","BK4585","BK4588","IE00BFXG1179.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2642448325","title":"Sanofi to Stop Late-Stage Study of Immune-Disorder Drug","url":"https://stock-news.laohu8.com/highlight/detail?id=2642448325","media":"Dow Jones","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2642448325?lang=en_us&edition=fundamental","pubTime":"2026-06-10 14:18","pubTimestamp":1781072280,"startTime":"0","endTime":"0","summary":"Sanofi said it would stop a late-stage study of an experimental treatment for a rare immune disorder after concluding the drug was unlikely to deliver sufficient efficacy.The French drugmaker said Wednesday that it would consider whether to continue other studies for the drug, riliprubart, currently under way.The study termination deals an early setback to Sanofi's newly appointed chief executive, Belen Garijo, who took the helm last month after leading Germany's Merck KGaA since 2021.The decision to stop the trial for riliprubart in patients with a rare neurological condition known as chronic inflammatory demyelinating polyneuropathy followed an interim analysis by an independent data-monitoring committee that showed the study was unlikely to achieve sufficient efficacy, the company said.The study evaluated whether patients who didn't respond to the standard-of-care therapy could be treated with riliprubart, which is designed to block an enzyme that drives key inflammatory mechanisms ","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://dowjonesnews.com/newdjn/logon.aspx?AL=N","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":["SNYNF","BK4588","IE00BFXG1179.USD","BK4585","SNY","BK4007"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2641438597","title":"European Equities Traded in the US as American Depositary Receipts Start Week Higher in Monday Trading","url":"https://stock-news.laohu8.com/highlight/detail?id=2641438597","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2641438597?lang=en_us&edition=fundamental","pubTime":"2026-06-08 23:10","pubTimestamp":1780931424,"startTime":"0","endTime":"0","summary":"European equities traded in the US as American depositary receipts kicked off the week higher late Monday morning, lifting 0.82% to 1,874.41 on the S&P Europe Select ADR Index.From continental Europe, the gainers were led by semiconductor company Sequans Communications  and biotech firm Evaxion , which rose 7% and 4.5% respectively. They were followed by accommodations booking company trivago  and telecommunications company Nokia , which increased 4.4% and 1.7% respectively.The decliners from continental Europe were led by pharmaceutical company Novo Nordisk  and biopharmaceutical company Cellectis , which fell 2.9% and 2.3% respectively. They were followed by pharmaceutical company Sanofi  and biopharmaceutical company Grifols , which were down 2% each.The gainers from the UK were led by biopharmaceutical companies Biodexa Pharmaceuticals  and NuCana , which advanced 4.5% and 3.3% respectively. They were followed by oil and gas company BP  and biopharmaceutical company Amarin , which ","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":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["AMRN","BK4588","BK4141","EVAX","BK4201","BK4139","IE00BKVL7J92.USD","NCNA","NVO","AUTL","LU1093756168.USD","LU1162221912.USD","CLLS","IE00BMPRXN33.USD","IE00BZ1G4Q59.USD","NGG","TRVG","BDRX","BPH","BK4077","LU1093756325.SGD","NVOH","BP","GSK","SNY","LU0300736492.USD","GSK.UK","IE00BFXG1179.USD","LU0006061336.USD","NVOX","BK4020","BK4505","MREO","BK4532","LU0162691827.USD","GSKH","BK4599","SQNS","BK4585","LU0154236417.USD","LNOK","NOK","LU1829250122.USD","BK4007","LU0300736062.USD","LU0320765646.SGD","IE00BMPRXR70.SGD","BK4208","LU0072461881.USD","GRFS","BK4547"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2641102297","title":"Sanofi's Subcutaneous Sarclisa Approved in EU Across Multiple Myeloma Indications","url":"https://stock-news.laohu8.com/highlight/detail?id=2641102297","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2641102297?lang=en_us&edition=fundamental","pubTime":"2026-06-08 16:34","pubTimestamp":1780907648,"startTime":"0","endTime":"0","summary":"Sanofi's  Sarclisa received European Commission's approval for its subcutaneous formulation across all European Union indications currently authorized for the intravenous treatment in multiple myeloma, the company said Monday.With the approval, Sarclisa becomes the first anticancer medicine in the EU available through an on-body injector, enabling treatment in outpatient clinics and patients' homes.The decision was supported by phase 3 IRAKLIA data showing that subcutaneous Sarclisa delivered via an on-body injector was non-inferior to the intravenous version in patients with relapsed or refractory multiple myeloma, Sanofi said.The company added that subcutaneous Sarclisa was associated with fewer systemic infusion reactions than the intravenous form, with no new safety concerns beyond mostly low-grade injection-site reactions.","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":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["SNYNF","BK4156","BK4585","SNY","BK4007","IE00BFXG1179.USD","BK4588"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1156905040","title":"Movement Alert｜Sanofi Rises 4.59% in Regular Trading, First-in-Class Drug Venglustat Granted FDA Priority Review for Rare Disease","url":"https://stock-news.laohu8.com/highlight/detail?id=1156905040","media":"Market Focus","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1156905040?lang=en_us&edition=fundamental","pubTime":"2026-06-04 22:06","pubTimestamp":1780582015,"startTime":"0","endTime":"0","summary":"On June 4, Sanofi rose 4.59% in regular trading, trading at $44.56/share, with trading volume of $27.25 million. The rally was driven by the announcement that its first-in-class drug Venglustat...","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","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":["SNY"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1142049791","title":"Movement Alert｜Sanofi Rises 3.09% in Pre-Market Trading, First-in-Class Drug Venglustat Granted FDA Priority Review","url":"https://stock-news.laohu8.com/highlight/detail?id=1142049791","media":"Market Focus","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1142049791?lang=en_us&edition=fundamental","pubTime":"2026-06-04 17:06","pubTimestamp":1780563974,"startTime":"0","endTime":"0","summary":"On June 4, Sanofi rose 3.09% in pre-market trading, trading at $43.68/share, with trading volume of $356,200. The move was driven by the announcement that its first-in-class therapy Venglustat has...","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"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":["SNY"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1153188711","title":"Sanofi's Groundbreaking Drug Venglustat Seeks FDA Approval for Type 3 Gaucher Disease","url":"https://stock-news.laohu8.com/highlight/detail?id=1153188711","media":"Stock News","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1153188711?lang=en_us&edition=fundamental","pubTime":"2026-05-28 21:20","pubTimestamp":1779974426,"startTime":"0","endTime":"0","summary":"On May 28, Sanofi announced that the U.S. Food and Drug Administration (FDA) has accepted and granted priority review for the New Drug Application (NDA) of Venglustat, intended for the treatment of...","market":"sg","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"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","159992","BK1574","BK1161","BK4588","BK4007","SNY","IPOS","06978","BK4585"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2638664549","title":"Sanofi announces FDA grants priority review to venglustat new drug application","url":"https://stock-news.laohu8.com/highlight/detail?id=2638664549","media":"TIPRANKS","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2638664549?lang=en_us&edition=fundamental","pubTime":"2026-05-28 17:59","pubTimestamp":1779962363,"startTime":"0","endTime":"0","summary":"The FDA has granted priority review to Sanofi’s (SNY) new drug application for venglustat, an investigational oral glucosylceramide synthase inhibi...","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/sanofi-announces-fda-grants-priority-review-to-venglustat-new-drug-application-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/sanofi-announces-fda-grants-priority-review-to-venglustat-new-drug-application-thefly-news?utm_source=itigerup.com&utm_medium=referral","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":"tipranks_highlight","symbols":["SNYNF","SNY","LABU","BK4588","BK4585","IE00BFXG1179.USD","BK4007"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2638668782","title":"Sanofi Granted FDA Priority Review for Potential Treatment of Rare Gaucher Disease","url":"https://stock-news.laohu8.com/highlight/detail?id=2638668782","media":"MT Newswires Live","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2638668782?lang=en_us&edition=fundamental","pubTime":"2026-05-28 15:37","pubTimestamp":1779953867,"startTime":"0","endTime":"0","summary":"Sanofi  has been granted US Food and Drug Administration priority review for a new drug application for venglustat for the treatment of type 3 Gaucher disease, a rare disorder, the company said Thursday.The application is backed by data from a phase 3 study in which venglustat met both its primary endpoints and three out of four key secondary endpoints, the drugmaker said.The target action date for the FDA decision is November 25, the company said.Gaucher disease results in an abnormal buildup of sugar-and-fat molecules in the spleen, liver, bone marrow, and lungs, potentially causing neurological and cognitive challenges.Sanofi will pursue more global regulatory filings for venglustat this year, it 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":"2","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["IE00BFXG1179.USD","SNY","BK4585","SNYNF","BK4588","LABU","BK4007"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2636006128","title":"Sanofi reports ElevAATe trial of efdoralprin alfa meets primary 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Pharmaceuticals Trial Miss May Raise Broader Strategy Questions, RBC Says","url":"https://stock-news.laohu8.com/highlight/detail?id=2636187072","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2636187072?lang=en_us&edition=fundamental","pubTime":"2026-05-18 23:11","pubTimestamp":1779117065,"startTime":"0","endTime":"0","summary":"Regeneron Pharmaceuticals' (REGN) fianlimab trial miss might lead some investors to question the company's broader strategy and execution, RBC Capital Markets said.The company reported late Friday 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