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Novartis AG

148.18

-1.5200-1.02%

Post-market: 148.180.00000.00%18:58 EDT

Volume:1.98M

Turnover:295.47M

Market Cap:282.73B

PE:20.72

High:150.60

Open:150.01

Low:147.86

Close:149.70

52wk High:170.46

52wk Low:97.72

Shares:1.91B

Float Shares:1.82B

Volume Ratio:1.37

T/O Rate:0.11%

Dividend:4.67

Dividend Rate:3.15%

EPS(TTM):7.15

EPS(LYR):7.15

ROE:30.81%

ROA:11.14%

PB:6.13

PE(LYR):20.72

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Overview Company News Filings

Novartis Says European Regulator Backs Expanded Use of Blood Cancer Drug

MT Newswires Live

Novartis Scemblix receives positive CHMP opinion for Scemblix

Small-Cap Biotech Climb Bio's Lead Drug Candidate Has Larger Long-Term Opportunity

Novartis' Phase 3 Study of Fabhalta in IgA Nephropathy Meets Primary Endpoint

MT Newswires Live

Novartis announces Phase III study of Fabhalta showed superiority to placebo

Novartis Growth Should Normalize After Successful Turnaround -- Market Talk

Novartis Growth Likely to Stall on Cosentyx Sales Slide -- Market Talk

Pharma Shares Rally. Eli Lilly Up Nearly 3%; Novo, Johnson & Johnson Up Around 2%; Sanofi, Pfizer, Astrazeneca Up Over 1%

Tiger Newspress

Immatics Names Venkat Ramanan CFO

MT Newswires Live

Novartis Receives FDA Approval for Skin Condition Treatment

MT Newswires Live

Novartis Bags First FDA Approval for Rhapsido, More Could Follow -- Market Talk

Novartis announces FDA approval of Rhapsido for treatment of CSU

Pharma's Direct-To-Patient Wave Hits Novartis Next

Benzinga_recent_news

Novartis to launch direct-to-patient platform for Cosentyx in U.S.

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Says European Regulator Backs Expanded Use of Blood Cancer Drug","url":"https://stock-news.laohu8.com/highlight/detail?id=2576703005","media":"MT Newswires Live","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2576703005?lang=en_us&edition=fundamental","pubTime":"2025-10-17 20:46","pubTimestamp":1760705185,"startTime":"0","endTime":"0","summary":"Novartis  said Friday that the Committee for Medicinal Products for Human Use of the European Medicines Agency has issued a positive opinion on Scemblix for the treatment of adult patients with Philadelphia chromosome-positive chronic myeloid leukemia in the chronic phase across all lines of treatment.The drugmaker said the recommendation was based on results from a phase III trial that demonstrated superior major molecular response rates, fewer dose reductions, and half the rate of treatment discontinuation due to side effects compared with the investigators' choice of tyrosine kinase inhibitor treatment in patients.The European Commission is expected to make a final decision on the CHMP recommendation within two months. If approved, Scemblix will be indicated for both newly diagnosed and previously treated adults, expanding access to four times as many patients in Europe, Novartis said.Scemblix is already approved for earlier-line use in over 20 countries, including the US, Japan, 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Scemblix","url":"https://stock-news.laohu8.com/highlight/detail?id=2576031359","media":"TIPRANKS","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2576031359?lang=en_us&edition=fundamental","pubTime":"2025-10-17 18:55","pubTimestamp":1760698518,"startTime":"0","endTime":"0","summary":"Novartis (NVS) announced that the Committee for Medicinal Products for Human Use, CHMP, of the European Medicines Agency, EMA, has adopted a positi...","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/novartis-scemblix-receives-positive-chmp-opinion-for-scemblix-thefly?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/novartis-scemblix-receives-positive-chmp-opinion-for-scemblix-thefly?utm_source=itigerup.com&utm_medium=referral","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":"tipranks_highlight","symbols":["CHMP","BK4087","IE00BFTCPJ56.SGD","LU0320765489.SGD","LU0211331839.USD","BK4532","IE00B2B36J28.USD","BK4007","IE0009355771.USD","LU0208291251.USD","BK4585","IE00BJJMRZ35.SGD","LU0070302665.USD","IE00BJT1NW94.SGD","BK4588","IE00B4R5TH58.HKD","IE0002141913.USD","BK4578","NVS"],"gpt_icon":0},{"id":"2576721761","title":"Small-Cap Biotech Climb Bio's Lead Drug Candidate Has Larger Long-Term Opportunity","url":"https://stock-news.laohu8.com/highlight/detail?id=2576721761","media":"Benzinga","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2576721761?lang=en_us&edition=fundamental","pubTime":"2025-10-17 01:40","pubTimestamp":1760636400,"startTime":"0","endTime":"0","summary":"William Blair assigns Climb Bio an Outperform rating, projecting peak sales of $1.9 billion and long-term growth for its therapy pipeline.","market":"nz","thumbnail":"https://cdn.benzinga.com/files/images/story/2025/10/16/Genetic-Research-And-Biotech-Science-Con.jpeg?optimize=medium&dpr=2&auto=webp&width=260","type":0,"news_type":0,"thumbnails":["https://cdn.benzinga.com/files/images/story/2025/10/16/Genetic-Research-And-Biotech-Science-Con.jpeg?optimize=medium&dpr=2&auto=webp&width=260"],"rights":{"source":"benzinga_hot_news","url":"https://www.benzinga.com/news/25/10/48258939/small-cap-biotech-climb-bios-lead-drug-candidate-has-larger-long-term-opportunity","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/25/10/48258939/small-cap-biotech-climb-bios-lead-drug-candidate-has-larger-long-term-opportunity","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":"benzinga_hot_news","symbols":["QID","SG9999001440.SGD","BK4533","IE00BJT1NW94.SGD","USAW.SI","NPV","BK4532","LU2089984988.USD","NQmain","AMGN","IE00BJJMRZ35.SGD","LU0208291251.USD","LU0058720904.USD","IE0009355771.USD","IE00B2B36J28.USD","BIIB","BK4588","IE0002141913.USD","LU1061106388.HKD","BK4534","USJW.SI","CTA","IE00B4R5TH58.HKD","CLYM","MNQmain","TQQQ","IE00B19Z9Z06.USD","IE00B19Z9P08.USD","NVIW.SI","NVS",".IXIC","BK4539","BK4007","LU0868494617.USD","LU2242646821.SGD","LU0234570918.USD","LU0109394709.USD","SQQQ","QLD","LU1023059063.AUD","TSYW.SI","BK4581","LU1571399168.USD","LU0211331839.USD","TGTX","PSQ","LU0122379950.USD","IE00BFTCPJ56.SGD","LU1057294990.SGD"],"gpt_icon":1},{"id":"2575881748","title":"Novartis' Phase 3 Study of Fabhalta in IgA Nephropathy Meets Primary Endpoint","url":"https://stock-news.laohu8.com/highlight/detail?id=2575881748","media":"MT Newswires Live","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2575881748?lang=en_us&edition=fundamental","pubTime":"2025-10-16 19:16","pubTimestamp":1760613415,"startTime":"0","endTime":"0","summary":"Novartis  said Thursday that its phase 3 study of Fabhalta in adults with IgA nephropathy kidney disease, or IgAn, met its primary endpoint.The achieved primary endpoint is a \"statistically significant\" improvement in estimated glomerular filtration rate, or eGFR, slope compared with placebo over two years, the company said, noting that eGFR is key marker of kidney function.Another primary endpoint is proteinuria reduction at nine months as measured by UPCR, according to Novartis.Novartis also said Fabhalta was well tolerated during the phase 3 trial, with a safety profile consistent with previously reported data.The company said it plans to use the trial's data to support submissions for Fabhalta in 2026.","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://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":["IE0002141913.USD","BK4007","IE00B2B36J28.USD","LU0070302665.USD","BK4578","BK4532","IE00BFTCPJ56.SGD","NVS","BK4588","IE00B4R5TH58.HKD","BK4585","IE00BJJMRZ35.SGD","IE00BJT1NW94.SGD","LU0211331839.USD","IE0009355771.USD","LU0320765489.SGD","LU0208291251.USD"],"gpt_icon":0},{"id":"2575175217","title":"Novartis announces Phase III study of Fabhalta showed superiority to placebo","url":"https://stock-news.laohu8.com/highlight/detail?id=2575175217","media":"TIPRANKS","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2575175217?lang=en_us&edition=fundamental","pubTime":"2025-10-16 18:36","pubTimestamp":1760610966,"startTime":"0","endTime":"0","summary":"Novartis (NVS) announced positive final results from APPLAUSE-IgAN, a Phase III study evaluating Fabhalta in adults living with IgA nephropathy, Ig...","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/novartis-announces-phase-iii-study-of-fabhalta-showed-superiority-to-placebo-thefly?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/novartis-announces-phase-iii-study-of-fabhalta-showed-superiority-to-placebo-thefly?utm_source=itigerup.com&utm_medium=referral","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":"tipranks_highlight","symbols":["IE00B2B36J28.USD","IE0002141913.USD","IE0009355771.USD","LU0208291251.USD","IE00B4R5TH58.HKD","BK4134","LU0320765489.SGD","III","BK4588","BK4585","NVS","BK4578","IE00BJJMRZ35.SGD","IE00BJT1NW94.SGD","LU0070302665.USD","BK4532","LU0211331839.USD","IE00BFTCPJ56.SGD","BK4007"],"gpt_icon":0},{"id":"2575204467","title":"Novartis Growth Should Normalize After Successful Turnaround -- Market Talk","url":"https://stock-news.laohu8.com/highlight/detail?id=2575204467","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2575204467?lang=en_us&edition=fundamental","pubTime":"2025-10-15 16:59","pubTimestamp":1760518740,"startTime":"0","endTime":"0","summary":"0859 GMT - Novartis completed a successful transformation and now outperforms its peers, but growth is set to normalize, Vontobel's Stefan Schneider writes. The Swiss pharma group's valuation now reflects its recent growth, though this happened more slowly than expected given nine straight quarters of Novartis beating and raising guidance, the analyst says. This is unlikely to be repeated when the company releases third-quarter results later this month, its first report since heart failure drug Entresto lost patent exclusivity, the analysts add. Novartis seems poised to deliver slower growth going forward, the analyst says. Vontobel cuts its recommendation on Novartis stock to hold from buy and keeps its target price of 112 Swiss francs. Shares fall 1.1% to 102.92 francs. 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Cosentyx U.S. sales are likely to drop 17% mainly due to increased competition and lower prices and compared with consensus forecasts for a 10% rise, the analysts say. The decrease could cut Novartis's EBIT by about 5%, they add. Together with the Swiss pharma group's Entresto heart-failure drug loss of patent exclusivity, this will likely lead to flat earnings per share next year, the analysts write. Moreover, Novartis's long-term revenue growth remains weak and lags that of other major European drugmakers, the analysts add. Intron Health cuts its recommendation on Novartis's stock to hold from buy. Shares fall 0.4% Monday and are up 18% year to date. 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Eli Lilly Up Nearly 3%; Novo, Johnson & Johnson Up Around 2%; Sanofi, Pfizer, Astrazeneca Up Over 1%","url":"https://stock-news.laohu8.com/highlight/detail?id=1179003778","media":"Tiger Newspress","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1179003778?lang=en_us&edition=fundamental","pubTime":"2025-10-03 22:49","pubTimestamp":1759502993,"startTime":"0","endTime":"0","summary":"Pharma shares rallied on Friday. Eli Lilly up nearly 3%; Novo, Johnson & Johnson up around 2%; Sanofi, Pfizer, AstraZeneca up over 1%.","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":"4696633c589b47e403d3f9d9fe1681de","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":true,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LLY","JNJ","NVS","MRNA","PFE","MRK","NVAX","NVO"],"gpt_icon":0},{"id":"2572350355","title":"Immatics Names Venkat Ramanan CFO","url":"https://stock-news.laohu8.com/highlight/detail?id=2572350355","media":"MT Newswires Live","labels":["executive"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2572350355?lang=en_us&edition=fundamental","pubTime":"2025-10-01 19:43","pubTimestamp":1759319014,"startTime":"0","endTime":"0","summary":"Immatics (IMTX) said Wednesday it has appointed Venkat Ramanan as its chief financial officer.Ramanan, who succeeds Arnd Christ, was previously the CFO of Anthos Therapeutics, which was acquired by Novartis (NVS) in April.","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":"executive","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["BK4532","BK4588","NVS","LU0070302665.USD","IE0002141913.USD","LU0211331839.USD","LU0320765489.SGD","IE0009355771.USD","IE00BJJMRZ35.SGD","BK4007","IE00BJT1NW94.SGD","BK4585","IE00BFTCPJ56.SGD","BK4139","BK4578","IMTX","IE00B4R5TH58.HKD","IE00B2B36J28.USD","LU0208291251.USD"],"gpt_icon":0},{"id":"2572584482","title":"Novartis Receives FDA Approval for Skin Condition Treatment","url":"https://stock-news.laohu8.com/highlight/detail?id=2572584482","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2572584482?lang=en_us&edition=fundamental","pubTime":"2025-10-01 16:34","pubTimestamp":1759307677,"startTime":"0","endTime":"0","summary":"Novartis  said late Tuesday the US Food and Drug Administration has approved Rhapsido for adult patients with chronic spontaneous urticaria who remain symptomatic despite H1 antihistamine treatment.Chronic spontaneous urticaria is a skin condition characterized by the appearance of itchy hives and swelling.The company said the approval was based on the results of two phase 3 trials, where Rhapsido demonstrated \"superiority\" in change from baseline, compared with placebo, in itch, hives, and weekly urticaria activity at week 12.","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":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["IE00BJT1NW94.SGD","BK4588","BK4578","IE0002141913.USD","LU0320765489.SGD","BK4532","IE0009355771.USD","IE00B4R5TH58.HKD","BK4585","NVS","LU0208291251.USD","IE00BJJMRZ35.SGD","LU0070302665.USD","LU0211331839.USD","IE00B2B36J28.USD","IE00BFTCPJ56.SGD","BK4007"],"gpt_icon":0},{"id":"2572586539","title":"Novartis Bags First FDA Approval for Rhapsido, More Could Follow -- Market Talk","url":"https://stock-news.laohu8.com/highlight/detail?id=2572586539","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2572586539?lang=en_us&edition=fundamental","pubTime":"2025-10-01 14:47","pubTimestamp":1759301220,"startTime":"0","endTime":"0","summary":"0646 GMT - Novartis's Rhapsido received approval from the U.S. Food and Drug Administration to treat hives, but the drug is also being evaluated in other conditions that could expand the company's immunology and neuroscience portfolios, Vontobel's Stefan Schneider says. Sales for Rhapsido--commercial name of the drug known until now as remibrutinib--in spontaneous hives, or urticaria, could hit $1.75 billion, according to Vontobel. The Swiss pharmaceutical company is also conducting trials for food allergy and other skin conditions that could expand its immunology portfolio, the analyst says in a research note. The drug is also being studied for multiple sclerosis and myasthenia, which could support growth in Novartis's neuroscience portfolio, he says. Line extensions are likely to make up a large chunk of Novartis's upcoming updates, Vontobel says. 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