BMY
Bristol-Myers Squibb Company · Healthcare · Drug Manufacturers - General
At close
$61.82
−$0.55 (−0.88%) Close
Pre-market $61.94 +$0.12 (+0.19%) 4:13 AM ET
Prev close $62.37
Open $62.16
Day high $62.16
Day low $61.51
Volume 4,450
Avg vol 13,418,646
Mkt cap
$127.01B
P/E ratio
17.92
FY Revenue
$48.19B
EPS
3.45
Gross Margin
71.08%
Sector
Healthcare
AI report sections
BMY
Bristol-Myers Squibb Company
Bristol-Myers Squibb is trading near the upper half of its 52-week range with solid 3–6 month price appreciation and bullish technical signals. Fundamentally, the company combines high margins, rising earnings, and strong free cash flow generation with elevated leverage and a sizeable long-term debt load. Valuation appears moderate on earnings and cash flow metrics while the short-interest profile remains low and not indicative of broad bearish positioning.
AI summarized at 7:21 PM ET, 2026-02-04
AI summary scores
INTRADAY: 63 SWING: 76 LONG: 82
Volume vs average
Intraday (cumulative)
+90% (Above avg)
Vol/Avg: 1.90×
RSI
64.13 (Strong)
Strong (60–70)
MACD momentum
Intraday
+0.03 (Strong)
MACD: 0.01 Signal: -0.02
Short-Term
-0.02 (Weak)
MACD: 1.51 Signal: 1.53
Long-Term
+0.08 (Strong)
MACD: 2.62 Signal: 2.53
Intraday trend score 71.56

Latest news

BMY 12 articles Positive: 6 Neutral: 6 Negative: 0
Positive The Motley Fool • Reuben Gregg Brewer
Big Pharma Dividend Stock BMY Could Help Turn $100,000 Into a Seven‑Figure Retirement

Bristol Myers Squibb offers an attractive 4% dividend yield, well above the S&P 500's 1.1% and pharma sector average of 1.7%. Trading 25% below late 2022 highs with a sustainable 70% payout ratio and strong dividend growth history, BMY could serve as a foundation for long-term wealth building through dividend reinvestment, despite current market focus on GLP-1 drugs and upcoming patent expirations.

BMY CELGR dividend stocks pharmaceutical companies dividend yield patent expiration dividend reinvestment retirement investing
Sentiment note

Company offers an attractive 4% dividend yield with a sustainable payout ratio of 70%, strong dividend growth history, and recovery potential as stock trades 25% below 2022 highs. While facing patent expiration challenges and market neglect due to GLP-1 hype, the company has proven ability to manage patent expirations and maintains a solid pipeline in cardiovascular, cancer, and immune-related medicines.

Neutral GlobeNewswire Inc. • Fight Colorectal Cancer (Fight Crc)
A Symbol of Crisis: As Colorectal Cancer Deaths Rise, Fight CRC Installs United in Blue on the National Mall

Fight Colorectal Cancer launches its fifth annual United in Blue installation on the National Mall from March 1-14, 2026, featuring over 27,000 blue flags representing people under 50 projected to be diagnosed with colorectal cancer in 2030. The installation comes as new American Cancer Society research confirms colorectal cancer has become the deadliest cancer for Americans under 50, with mortality increasing in 2025.

AMGN BMY CELGR JNJ colorectal cancer cancer awareness United in Blue National Mall
Sentiment note

Sponsor of the awareness campaign, suggesting commitment to oncology and cancer research, but no direct business implications discussed.

Neutral GlobeNewswire Inc. • Spherix Global Insights
One in Three Rheumatologists View BMS’ Sotyktu as a Substantial Advance in Psoriatic Arthritis Ahead of March 6 FDA Decision, According to Spherix Global Insights Data

Ahead of the March 6, 2026 FDA decision on Bristol Myers Squibb's Sotyktu (deucravacitinib) for psoriatic arthritis, a survey of 104 U.S. rheumatologists shows strong pre-launch awareness with one-third viewing it as a substantial advance. However, BMS ranks lowest among major pharmaceutical partners in rheumatology and is expected to capture roughly one-fifth of PsA patients through brand-to-brand share shifts rather than market expansion. The launch represents a critical opportunity for BMS to strengthen its standing in the specialty.

BMY CELGR PFE ABBV psoriatic arthritis TYK2 inhibitor FDA approval rheumatology
Sentiment note

While Sotyktu shows strong pre-launch awareness and one-third of rheumatologists view it as a substantial advance, BMS faces significant headwinds. The company ranks lowest among major pharmaceutical partners in rheumatology, lacks differentiation on key support metrics, and is expected to compete through brand-to-brand share shifts rather than market expansion. The launch is positioned as a critical opportunity to improve BMS's standing, suggesting current perception challenges outweigh the positive product reception.

Positive Benzinga • Vandana Singh
Bristol Myers Says New Breast Cancer Drug Shows Survival Benefit In Pretreated Patients

Bristol Myers Squibb announced positive interim Phase 3 trial results for izalontamab brengitecan (Iza-bren), a breast cancer drug developed with SystImmune, showing statistically significant improvements in progression-free and overall survival for triple-negative breast cancer patients. Despite the positive clinical data, BMY shares declined 0.56% on Thursday, trading below key moving averages with mixed technical indicators.

BMY CELGR breast cancer Phase 3 trial izalontamab brengitecan triple-negative breast cancer survival benefit Breakthrough Therapy Designation
Sentiment note

The company announced positive Phase 3 trial results meeting dual primary endpoints for a new breast cancer drug with statistically significant survival improvements. The drug has received Breakthrough Therapy Designation from FDA and China's NMPA. This represents meaningful clinical progress for an important indication with limited treatment options.

Neutral GlobeNewswire Inc. • Bcc Research
Advanced Drug Delivery Market to Grow 10.2% Annually Through 2030

The global Advanced Drug Delivery Systems market is projected to grow from $299.6 billion in 2025 to $487.4 billion by 2030 at a CAGR of 10.2%. Growth is driven by increasing chronic disease prevalence, nanotechnology advances, and R&D investments. Oncology leads adoption, with North America dominating market share while Asia-Pacific shows the fastest growth. Key innovations include strategic partnerships in antibody-drug conjugates and AI-powered drug development optimization.

GILD ABBV AMGN JNJ Advanced Drug Delivery Systems Nanotechnology Oncology Antibody-Drug Conjugates
Sentiment note

Listed as a market leader but no specific innovations or developments mentioned in the article.

Neutral GlobeNewswire Inc. • Na
Kyverna Therapeutics Appoints Biotech Leaders Sravan Emany and Andrew Miller to Board of Directors

Kyverna Therapeutics announced the appointments of Sravan K. Emany and Andrew Miller to its Board of Directors as the company advances toward commercialization of its cell therapies for autoimmune diseases. Emany, currently CFO of Beam Therapeutics, brings capital markets and rare disease expertise, while Miller, a Time Magazine honoree and former Karuna Therapeutics leader, adds clinical development and product approval experience. Dan Spiegelman has stepped down from the Board.

KYTX BEAM BMY CELGR board appointments cell therapy autoimmune diseases commercialization
Sentiment note

Mentioned only in context of acquiring Karuna Therapeutics in 2024. No direct impact or strategic implications are discussed in relation to this announcement.

Positive Benzinga • Vandana Singh
Bristol-Myers Touts Promising Data From Blood Disorder Study

Bristol-Myers Squibb announced positive topline results from a Phase 2 study of Reblozyl for treating Alpha-Thalassemia, an inherited blood disorder. The study met its primary endpoints, showing significant increases in hemoglobin levels and reduced transfusion burden. The company plans to present results at a medical congress and discuss findings with Chinese regulators. BMY stock was up 0.78% at $61.14 at publication.

BMY CELGR Reblozyl Alpha-Thalassemia Phase 2 study blood disorder hemoglobin clinical trial
Sentiment note

The company announced successful Phase 2 trial results meeting primary and secondary endpoints for Reblozyl in treating Alpha-Thalassemia. This represents meaningful clinical progress for a drug addressing an unmet medical need with limited treatment options. The positive data supports potential regulatory approval and market expansion, particularly in China.

Neutral GlobeNewswire Inc. • Na
Starton Therapeutics Announces Dosing of First Patient in Phase 2a Study Evaluating STAR-LLD for the Treatment of Multiple Myeloma

Starton Therapeutics announced the dosing of the first patient in its Phase 2a clinical trial for STAR-LLD, a continuous subcutaneous delivery formulation of lenalidomide designed to treat relapsed/refractory multiple myeloma. The study will enroll 24 patients with an option to expand to 69 patients, comparing three doses of STAR-LLD against oral Revlimid. The trial has expanded from two to six investigational sites across the United States, with enrollment expected to complete in the first half of 2027.

BMY CELGR STAR-LLD lenalidomide multiple myeloma Phase 2a trial continuous delivery clinical development
Sentiment note

Revlimid (lenalidomide) is mentioned as the comparator drug in the trial. While STAR-LLD aims to improve upon oral Revlimid's tolerability profile, this represents potential competition rather than direct negative impact on the company's current operations or market position.

Positive GlobeNewswire Inc. • Researchandmarkets.Com
CTLA-4 Inhibitors Competitive Landscape Research Report 2026: Comprehensive Insights About 40+ Companies and 50+ Drugs by Product Type, Stage, Route of Administration, and Molecule Type

A comprehensive market report reveals over 40 companies developing 50+ CTLA-4 inhibitor drugs for cancer immunotherapy. Key developments include FDA approvals for tremelimumab in hepatocellular cancer and MT-8421 for solid tumors, along with promising clinical progress from multiple biopharmaceutical companies in checkpoint inhibitor combinations and bispecific antibodies.

BMY CELGR IVBIY AGEN CTLA-4 inhibitors cancer immunotherapy checkpoint inhibitors bispecific antibodies
Sentiment note

Established market presence with Yervoy, an approved CTLA-4 monoclonal antibody expanding across multiple tumor types, demonstrating commercial success and broad therapeutic potential.

Positive GlobeNewswire Inc. • Researchandmarkets.Com
Checkpoint Inhibitors Competitive Landscape Report 2026: Comprehensive Insights About 50+ Companies and 60+ Drugs

A comprehensive market report on checkpoint inhibitors covering 50+ companies and 60+ drugs in oncology. The report highlights key players like Bristol Myers Squibb, Genentech, and emerging companies such as OncoC4 and Transcode Therapeutics, with analysis of marketed therapies, pipeline products, and recent industry collaborations and acquisitions in the immuno-oncology space.

BMY CELGR KYKOY RNAZ checkpoint inhibitors immuno-oncology cancer immunotherapy PD-1
Sentiment note

Recognized as a leader in biopharmaceuticals with Opdivo, a successful marketed checkpoint inhibitor with significant global approval, demonstrating strong expertise in immuno-oncology.

Neutral GlobeNewswire Inc. • Sns Insider
Hepatitis B Treatment Market Size is Projected to Reach USD 7.74 Billion by 2033 Due to the Increasing Disease Management Trends Globally

The global Hepatitis B treatment market is valued at USD 4.52 billion in 2025 and is projected to reach USD 7.74 billion by 2033, growing at a CAGR of 6.97%. Growth is driven by expanded screening programs, increased antiviral therapy adoption, and novel treatment innovations. The U.S. market is expected to grow from USD 1.00 billion to USD 1.54 billion by 2033.

GILD GSK BMY CELGR Hepatitis B treatment antiviral drugs screening programs RNA interference therapies
Sentiment note

Listed as a major player in the hepatitis B treatment market but no specific recent developments or clinical data mentioned in the article.

Positive GlobeNewswire Inc. • Delveinsight
Idiopathic Pulmonary Fibrosis Clinical Trials & Pipeline Overview: Insights into 80+ Leading Companies and 100+ Novel Treatments | DelveInsight

The idiopathic pulmonary fibrosis (IPF) treatment landscape is expanding with 80+ companies developing 100+ novel therapies across various clinical stages. Growing disease awareness and diagnostic improvements are driving demand for more effective treatments beyond current antifibrotic limitations. Key developments include orphan drug designations, positive clinical trial data, and FDA clinical hold lifts for several promising candidates in 2025-2026.

BMY CELGR RHHBY TVRD idiopathic pulmonary fibrosis IPF clinical trials pipeline therapies
Sentiment note

Leading company with BMS-986278 in Phase III trials for IPF, indicating advanced stage development and strong pipeline presence in growing market

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