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Bristol-Myers Squibb

59.70

+0.11000.18%

Post-market: 59.67-0.0300-0.05%18:08 EDT

Volume:11.09M

Turnover:662.02M

Market Cap:121.53B

PE:13.14

High:60.10

Open:59.45

Low:59.01

Close:59.59

52wk High:68.64

52wk Low:42.52

Shares:2.04B

Float Shares:2.03B

Volume Ratio:0.84

T/O Rate:0.55%

Dividend:2.51

Dividend Rate:4.20%

EPS(TTM):4.54

EPS(LYR):3.46

ROE:46.60%

ROA:10.72%

PB:5.45

PE(LYR):17.25

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Overview Company News Filings

Bayer Bets $2.2 Billion That America Is Still The Best Place To Make Drugs

23.3% Vs 14.8%: Lilly's New Data Just Changed The Obesity Drug Playbook

Bellwether Stocks Movement

Perspective Therapeutics [212Pb]VMT01 Melanoma Trial Data Set for SITC 2026 Presentation

Major Drugmakers Turn to China for Licensing Deals

Novartis Bets $7.8 Billion On MRNA Beyond Vaccines

Options & Short Sell

Bristol Myers Squibb Co. Stock Outperforms Competitors Despite Losses on the Day

BMY Terminates Early Leukemia Trial, Trimming One Risky Bet From Its Oncology Pipeline

InflaRx Appoints Gabriela Alperovich as SVP, Global Head of Clinical Development

Iovance Biotherapeutics Names Noah Berkowitz Chief Medical Officer

Bristol Myers Squibb Deepens Commitment to Healthcare Professionals Through Champions in Care Movement

THOMSON REUTERS

Sanofi’s Regeneron Fix Requires Extra Shot of M&A

Bayer Names Christoph Koenen Chief Medical Officer

Faron Pharmaceuticals Doses First Patient in Phase 1/2 BLAZE Trial of Bexmarilimab Plus Bristol Myers’ Opdivo in PD-1-Resistant Solid Tumors

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

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Stock Outperforms Competitors Despite Losses On The DayThis article was automatically generated by MarketWatch using technology from Automated Insights.Shares of Bristol Myers Squibb Co.  slipped 1.51% to $61.46 Thursday, on what proved to be an all-around positive trading session for the stock market, with the S&P 500 Index  rising 0.19% to 7,666.45 and the Dow Jones Industrial Average  rising 0.04% to 50,926.56.This was the stock's third consecutive day of losses.Bristol Myers Squibb Co. closed 10.46% short of its 52-week high of $68.64, which the company achieved on August 19th.The stock demonstrated a mixed performance when compared to some of its competitors Thursday, as Johnson & Johnson  fell 2.30% to $258.66, Pfizer Inc.  fell 1.40% to $28.12, and Abbott Laboratories  fell 2.17% to $96.69.Trading volume  remained 507,251 below its 50-day average volume of 11.2 M.Data source: Dow Jones Market Data, FactSet. 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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 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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":["LU0237698245.USD","LU2242646821.SGD","LU1323610961.USD","LU1883839398.USD","BK4585","LU1868837136.USD","LU1868836757.USD","LU1989771016.USD","LU0225771236.USD","IHE","LU0306807586.USD","FTXH","BMY","LU1291159041.SGD","LU1718418525.SGD","BK4581","LU0061475181.USD","IE00BFXG1179.USD","BK4126","LU0306806265.USD","LU1430594728.SGD","LU0432979614.USD","LU2125154778.USD","LABU","LU0114720955.EUR","LU2596442595.SGD","IE0002141913.USD","LU1074936037.SGD","IE0009355771.USD","IE00B2B36J28.USD","IE00BJT1NW94.SGD","LU1093756168.USD","IE00BSNM7G36.USD","LU1670711040.USD","BK4534","BK4588","LU1236620750.USD","LU0868494617.USD","LU1585245621.USD","BK4559","LU0096364046.USD","MYE","LU2360032135.SGD","BK4007","LU0225284248.USD","LU2242652126.USD","IE00BFTCPJ56.SGD","LU1868836914.USD","LU1868837300.USD","LU1571399168.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 monitoring. 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":"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":["LU1868836591.USD","LU1983299246.USD","IE00B2B36J28.USD","LU1571399168.USD","LU1430594728.SGD","BK4007","IE00BFTCPJ56.SGD","LU0114720955.EUR","LU1718418525.SGD","IE00BFXG1179.USD","IE00BJT1NW94.SGD","BK4126","LU0225284248.USD","BMY","LU0237698245.USD","LU2360032135.SGD","BK4534","LU0225771236.USD","MYE","BK4581","LU0061475181.USD","IE00BSNM7G36.USD","LU0985481810.HKD","LU0096364046.USD","LU1032466523.USD","LU1093756325.SGD","LU0321505439.SGD","LU1868837136.USD","IE00BJJMRZ35.SGD","BK4585","LU1868837300.USD","LU1670711040.USD","LU2596442595.SGD","FTXH","LU1261432733.SGD","BK4559","IE0002141913.USD","LU0306806265.USD","BK4532","LU1236620750.USD","LU1989771016.USD","IHE","LU0321505868.SGD","LU1236620834.HKD","LU1670710588.SGD","LU1868836914.USD","LU0432979614.USD","LU0267386448.USD","LU1093756168.USD","LU1074936037.SGD"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":10,"pageCount":2,"totalSize":200,"code":"91000000","status":"200"}]}}