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Bristol-Myers Squibb

62.40

-0.4600-0.73%

Post-market: 63.000.6000+0.96%18:11 EDT

Volume:15.87M

Turnover:998.88M

Market Cap:127.03B

PE:13.74

High:64.13

Open:63.28

Low:62.40

Close:62.86

52wk High:68.64

52wk Low:42.52

Shares:2.04B

Float Shares:2.03B

Volume Ratio:1.11

T/O Rate:0.78%

Dividend:2.51

Dividend Rate:4.02%

EPS(TTM):4.54

EPS(LYR):3.46

ROE:46.60%

ROA:10.72%

PB:5.69

PE(LYR):18.03

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Overview Company News Filings

U.S. Food and Drug Administration Approves Expanded Indication for Bristol Myers Squibb’s Camzyos® (Mavacamten) for the Treatment of Symptomatic Obstructive Hypertrophic Cardiomyopathy (Ohcm) in Adults and Pediatric Patients*

THOMSON REUTERS

Bristol-Myers Squibb's Camzyos to Treat Heart Condition Receives FDA Approval for Pediatric Patients

MT Newswires Live

FDA: Approved Camzyos (Mavacamten) Capsules as First Treatment for Children with Symptomatic Obstructive Hypertrophic Cardiomyopathy - Website

THOMSON REUTERS

FDA Approves First Drug to Improve Functional Capacity and Symptoms in Children with Rare Inherited Heart Condition

THOMSON REUTERS

FDA: Camzyos Carries Boxed Warning for Heart Failure Risk, Restricted to Rems Program

THOMSON REUTERS

FDA approves Bristol Myers’ Camzyos capsules for children with oHCM

Bristol-Myers' Protocol Changes Add Risk, Keep Admilparant on Track, UBS Says

MT Newswires Live

BMY Expands Real-World Cancer Data With New AUGTYRO Study in Korea

Pharma Sector Doubles Down on AI to Slash Costs, Timelines

Helix BioPharma Names Karen Krumeich Board Chair, Adds Three Directors

Bristol Myers Squibb Co. Stock Outperforms Competitors on Strong Trading Day

US Drugmakers Turn to China for Licensing Deals

Bristol Myers Squibb Co. Stock Outperforms Competitors on Strong Trading Day

Bristol-Myers Squibb Says Zenbexus Combination Doubles MRD-Negative Complete Response in Multiple Myeloma Trial

MT Newswires Live

Bristol Myers reports results from prespecified analysis of EXCALIBER-RRMM trial

Bristol Myers Squibb Wins FDA Accelerated Approval for Zenbexus Combo in Multiple Myeloma

Bristol Myers Squibb Announces First Presentation of Results for Zenbexus™ (Iberdomide) in Combination with Daratumumab from Phase 3 Excaliber-Rrmm Trial in Relapsed or Refractory Multiple Myeloma

THOMSON REUTERS

BMY’s Lung Cancer Combo Study Completion Adds Quiet Support to Its Immuno-Oncology Pipeline

Pharmaceutical Stocks Jump. Moderna, Eli Lilly up over 3%; Novavax, Pfizer up Around 2%; Merck, Novo Nordisk up over 1%

Tiger Newspress

RBC Capital Sticks to Their Hold Rating for Bristol-Myers Squibb (BMY)

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Squibb's Camzyos to Treat Heart Condition Receives FDA Approval for Pediatric Patients","url":"https://stock-news.laohu8.com/highlight/detail?id=2672784579","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2672784579?lang=en_us&edition=fundamental","pubTime":"2026-10-01 03:22","pubTimestamp":1790796162,"startTime":"0","endTime":"0","summary":"Bristol-Myers Squibb's  Camzyos to treat symptomatic obstructive hypertrophic cardiomyopathy was approved by the US Food and Drug Administration for use in pediatric patients, the agency said in a statement Wednesday.Camzyos, which was first approved for adults in 2022, is now approved for both adults and pediatric patients with weight of at least 30 kg with symptomatic oHCM, a genetically inherited condition that causes thickened heart muscle.The company's phase 3 efficacy data revealed improved left ventricular outflow tract obstruction in participants suffering from the heart condition, according to the statement.Camzyos received orphan drug designation for this indication, according to the agency.Price: 62.85, Change: -0.02, Percent Change: 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approves Bristol Myers’ Camzyos capsules for children with oHCM","url":"https://stock-news.laohu8.com/highlight/detail?id=2672781299","media":"TIPRANKS","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2672781299?lang=en_us&edition=fundamental","pubTime":"2026-10-01 02:35","pubTimestamp":1790793349,"startTime":"0","endTime":"0","summary":"The U.S. Food and Drug Administration approved Bristol Myers (BMY)’ Camzyos capsules as the first treatment for children with symptomatic obstructi...","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/fda-approves-bristol-myers-camzyos-capsules-for-children-with-ohcm-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/fda-approves-bristol-myers-camzyos-capsules-for-children-with-ohcm-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":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["BMY","LU0061475181.USD","IE00BSNM7G36.USD","LU1883839398.USD","IE0002141913.USD","BK4126","LU0225284248.USD","LU0114720955.EUR","BK4588","LU1074936037.SGD","LU1989771016.USD","LU2125154778.USD","BK4581","LU0432979614.USD","IE00BFTCPJ56.SGD","LU1718418525.SGD","LU0868494617.USD","LU1323610961.USD","LU1236620750.USD","LU1430594728.SGD","IE00BJT1NW94.SGD","LU1571399168.USD","LU1585245621.USD","LU1868836757.USD","LU1868837136.USD","LU2596442595.SGD","BK4559","IE00BFXG1179.USD","LU0096364046.USD","LU2242646821.SGD","IE00B2B36J28.USD","MYE","FTXH","BK4585","IE0009355771.USD","LU0225771236.USD","IHE","LU1093756168.USD","LU2360032135.SGD","LU1670711040.USD","LU0306807586.USD","BK4007","BK4534","LU1868837300.USD","LU2242652126.USD","LABU","LU1868836914.USD","LU0237698245.USD","LU1291159041.SGD","LU0306806265.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2672795786","title":"Bristol-Myers' Protocol Changes Add Risk, Keep Admilparant on Track, UBS Says","url":"https://stock-news.laohu8.com/highlight/detail?id=2672795786","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2672795786?lang=en_us&edition=fundamental","pubTime":"2026-10-01 00:34","pubTimestamp":1790786056,"startTime":"0","endTime":"0","summary":"Bristol-Myers Squibb's  protocol updates to the phase 3 long-term extension study of admilparant in idiopathic pulmonary fibrosis introduce some added risk while maintaining a favorable overall risk-benefit profile, UBS Securities said Tuesday in a report.The updates, issued in May, describe a small number of mild or short-lived liver-test abnormalities and one fatal case of multiorgan failure in a patient with several other medical complications, the report said.UBS said it is unclear whether the fatal case was caused by the drug, and there is no indication at this stage that treatment would require additional liver 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The updated protocol now includes routine testing, which is common in idiopathic pulmonary fibrosis studies, the report said.UBS said the key determinant will be the magnitude of efficacy in the upcoming phase 3 readout, expected in Q4 and likely in October.UBS has a buy rating on Bristol-Myers stock and an $80 price target.Price: 62.90, Change: +0.04, Percent ","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["LU0321505439.SGD","LU0432979614.USD","LU1571399168.USD","LU1868837136.USD","LU2596442595.SGD","BK4559","LU1670710588.SGD","LU0985481810.HKD","LU1718418525.SGD","LU1868837300.USD","BK4581","LU1032466523.USD","LU1989771016.USD","LU0321505868.SGD","LU0061475181.USD","IE00B2B36J28.USD","BK4126","LU1093756325.SGD","LU1236620750.USD","IE00BJT1NW94.SGD","LU1430594728.SGD","BK4007","IE0002141913.USD","BK4585","IE00BFTCPJ56.SGD","LU2360032135.SGD","LU1074936037.SGD","BK4532","LU1868836914.USD","LU1868836591.USD","LU1236620834.HKD","LU1670711040.USD","BK4534","LU1261432733.SGD","IHE","LU0225284248.USD","LU0306806265.USD","LU0267386448.USD","IE00BSNM7G36.USD","FTXH","LU0096364046.USD","LU0114720955.EUR","BMY","MYE","IE00BFXG1179.USD","IE00BJJMRZ35.SGD","LU0225771236.USD","LU0237698245.USD","LU1093756168.USD","LU1983299246.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2672786098","title":"BMY Expands Real-World Cancer Data With New AUGTYRO Study in Korea","url":"https://stock-news.laohu8.com/highlight/detail?id=2672786098","media":"TIPRANKS","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2672786098?lang=en_us&edition=fundamental","pubTime":"2026-10-01 00:31","pubTimestamp":1790785897,"startTime":"0","endTime":"0","summary":"Bristol-Myers Squibb Company ($BMY) announced an update on their ongoing clinical study. Bristol-Myers Squibb (BMY) is launching a post-marketing 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Myers Squibb Co. Stock Outperforms Competitors on Strong Trading Day","url":"https://stock-news.laohu8.com/highlight/detail?id=2671250966","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2671250966?lang=en_us&edition=fundamental","pubTime":"2026-09-29 04:37","pubTimestamp":1790627820,"startTime":"0","endTime":"0","summary":"DJ Bristol Myers Squibb Co. Stock Outperforms Competitors On Strong Trading DayThis article was automatically generated by MarketWatch using technology from Automated Insights.Shares of Bristol Myers Squibb Co.  rose 1.62% to $63.88 Monday, on what proved to be an all-around poor trading session for the stock market, with the S&P 500 Index  falling 0.77% to 7,683.69 and Dow Jones Industrial Average  falling 0.67% to 51,481.51.This was the stock's third consecutive day of gains.Bristol Myers Squibb Co. closed 6.93% short of its 52-week high of $68.64, which the company reached on August 19th.The stock outperformed some of its competitors Monday, as Johnson & Johnson  rose 0.27% to $271.95, Pfizer Inc.  rose 0.17% to $28.72, and Abbott Laboratories  fell 0.31% to $100.98.Trading volume  eclipsed its 50-day average volume of 10.9 M.Data source: Dow Jones Market Data, FactSet. Data compiled September 28, 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Drugmakers Turn to China for Licensing Deals","url":"https://stock-news.laohu8.com/highlight/detail?id=2670255552","media":"Reuters","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2670255552?lang=en_us&edition=fundamental","pubTime":"2026-09-28 22:31","pubTimestamp":1790605880,"startTime":"0","endTime":"0","summary":"FACTBOX-US drugmakers turn to China for licensing dealsSept 28 (Reuters)-MerckMRK.Non Monday agreed to payChinese biotechSciBrunch Therapeutics $400 million upfront for global rights to an 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Myers Squibb Co. Stock Outperforms Competitors on Strong Trading Day","url":"https://stock-news.laohu8.com/highlight/detail?id=2670242194","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2670242194?lang=en_us&edition=fundamental","pubTime":"2026-09-26 04:37","pubTimestamp":1790368620,"startTime":"0","endTime":"0","summary":"DJ Bristol Myers Squibb Co. Stock Outperforms Competitors On Strong Trading DayThis article was automatically generated by MarketWatch using technology from Automated Insights.Shares of Bristol Myers Squibb Co.  rose 2.21% to $62.86 Friday, on what proved to be an all-around favorable trading session for the stock market, with the S&P 500 Index  rising 0.51% to 7,743.41 and the Dow Jones Industrial Average  rising 0.93% to 51,828.62.This was the stock's second consecutive day of gains.Bristol Myers Squibb Co. closed 8.42% short of its 52-week high of $68.64, which the company achieved on August 19th.The stock outperformed some of its competitors Friday, as Johnson & Johnson  rose 0.20% to $271.22, Pfizer Inc.  rose 0.92% to $28.67, and Abbott Laboratories  rose 0.22% to $101.29.Trading volume  remained 832,136 below its 50-day average volume of 10.9 M.Data source: Dow Jones Market Data, FactSet. Data compiled September 25, 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Squibb Says Zenbexus Combination Doubles MRD-Negative Complete Response in Multiple Myeloma Trial","url":"https://stock-news.laohu8.com/highlight/detail?id=2670425385","media":"MT Newswires Live","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2670425385?lang=en_us&edition=fundamental","pubTime":"2026-09-25 23:10","pubTimestamp":1790349013,"startTime":"0","endTime":"0","summary":"Bristol-Myers Squibb  said Friday its Zenbexus treatment combination doubled the rate of minimal residual disease-negative complete response versus the daratumumab, bortezomib, and dexamethasone regimen in a phase 3 trial of relapsed or refractory multiple myeloma.After a median follow-up of 15.7 months, 41.1% of patients receiving Zenbexus with daratumumab and dexamethasone achieved an MRD-negative complete response rate of 41.1% versus 20.7% for those receiving daratumumab, bortezomib and dexamethasone, the company said.The overall response rate was 88.9% for the Zenbexus combination compared with 76.1% for the DVd regimen, Bristol-Myers Squibb said.The trial's other primary endpoint, progression-free survival, remains under evaluation in a confirmatory cohort of 800 patients, the company said.The US Food and Drug Administration granted accelerated approval in August to Zenbexus combined with daratumumab and hyaluronidase-fihj and dexamethasone for the treatment of adults with 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