BMY
HealthcareBristol Myers Squibb
Price Chart
Market Data
Financials
XBRL · SEC EDGAR2017–2025(9yr)| Metric | FY 2017 | FY 2018 | FY 2019 | FY 2020 | FY 2021 | FY 2022 | FY 2023 | FY 2024 | FY 2025Latest | YoY |
|---|---|---|---|---|---|---|---|---|---|---|
| Revenue | $20.8B | $22.6B | $26.1B | $42.5B | $46.4B | $46.2B | $45.0B | $48.3B | $48.2B | -0.2% |
| Gross Profit | $14.7B | $16.0B | $18.1B | $30.7B | $36.4B | $36.0B | $34.3B | $34.3B | $34.3B | -0.2% |
| Gross Margin | 70.8% | 71.0% | 69.1% | 72.3% | 78.6% | 78.0% | 76.2% | 71.1% | 71.1% | +0.0pp |
| Net Income | $1.0B | $4.9B | $3.4B | -$9.0B | $7.0B | $6.3B | $8.0B | -$8.9B | $7.1B | +178.8% |
| Net Margin | 4.8% | 21.8% | 13.2% | -21.2% | 15.1% | 13.7% | 17.8% | -18.5% | 14.6% | +33.2pp |
| Free Cash Flow | $4.2B | $5.0B | $7.2B | $13.3B | $15.2B | $11.9B | $12.7B | $13.9B | $12.8B | -7.9% |
| FCF Margin | 20.3% | 22.1% | 27.7% | 31.3% | 32.8% | 25.9% | 28.1% | 28.9% | 26.7% | -2.2pp |
| EPS (Diluted) | $0.61 | $3.01 | $2.01 | $-3.99 | $3.12 | $2.95 | $3.86 | $-4.41 | $3.46 | +178.5% |
1. THE BIG PICTURE
Bristol Myers Squibb is currently a tale of two portfolios: a shrinking legacy business that still pays the bills and a high-growth "new" business that isn't yet large enough to move the needle on total revenue. Bristol Myers Squibb is effectively a melting ice cube attempting to refreeze itself through aggressive R&DR&DResearch & Development — spending on creating new products or technologies and acquisitions, trading the reliable but doomed cash flows of drugs like Eliquis and Revlimid for a complex pipeline of CAR-T and radiopharmaceutical therapies.
2. WHERE THE RISKS HIT HARDEST
Bristol Myers Squibb’s "Operational Scale" is directly threatened by "Pricing and Reimbursement Controls" because its most successful products are the primary targets for government intervention. For example, Eliquis—a pillar of the legacy portfolio—is specifically named as subject to the Inflation Reduction Act’s "maximum fair prices" (10-K Item 1A). This regulatory pressure hits at the same time the product faces "Loss of Market Exclusivity," where generic competition typically triggers "substantial and rapid declines" in sales (10-K Item 1).
Furthermore, Bristol Myers Squibb’s "Strategic Business Development" strength is undermined by its "Concentration of Revenue." Because a majority of earnings come from a few key products like Opdivo and Eliquis, any single regulatory setback or clinical trial failure in the pipeline becomes a material threat to Bristol Myers Squibb’s ability to fund its 17th consecutive year of dividend increases (8-K, 10-K Item 1A).
3. WHAT THE NUMBERS SAY TOGETHER
The financial data reveals a company treading water. While the Growth Portfolio surged 16% in the most recent quarter, total revenue only grew by 1% because the Legacy Portfolio collapsed by 15% (8-K). This divergence explains why Bristol Myers Squibb ranks last among its peers in TTMTTMTrailing Twelve Months — the most recent full year of financial data, updated on a rolling basis each quarter revenue growth at -0.2% (XBRL). However, Bristol Myers Squibb remains a cash-generation machine, boasting a 34.7% Free Cash Flow (FCFFCFFree Cash Flow — cash left after paying for operations and capital investments; what the company can actually spend, save, or return to shareholders) margin—the second-highest in its peer group (XBRL).
This high FCFFCFFree Cash Flow — cash left after paying for operations and capital investments; what the company can actually spend, save, or return to shareholders provides the "strategic flexibility" management cites to invest in its "data-rich" 2026 pipeline (8-K). The market’s current lack of confidence is visible in the valuation; despite the high cash conversion, Bristol Myers Squibb trades at a significant discount to peers, likely because investors are focused on the $37.5 billion in net debt and the looming patent cliffs rather than the current yield (XBRL).
4. IS IT WORTH IT AT THIS PRICE?
At a 9.8x Forward P/EP/EPrice-to-Earnings ratio — share price divided by annual earnings per share; how much investors pay per dollar of profit. Higher P/E = higher growth expectations, Bristol Myers Squibb trades at a 36% discount to the peer median of 15.4x (XBRL). The market is pricing in a long-term growth rate of just 0.5% (CAPM analysis). This low bar appears attractively valued given that management is guiding for 2026 revenues of up to $47.5 billion and a non-GAAPGAAPGenerally Accepted Accounting Principles — the standard U.S. accounting rules all public companies must follow EPSEPSEarnings Per Share — the company's net profit divided by its share count; the most common per-share profitability metric of up to $6.35 (8-K).
However, the discount is justified by the structural risk of the "Legacy Portfolio" drag. For the current price to be "right," the Growth Portfolio must not only continue its 16% trajectory but also expand its margins to match the 28.3% net margins seen at peers like Merck (XBRL). Currently, Bristol Myers Squibb’s net margin of 15.1% is near the bottom of its peer group, suggesting that the "biotech-like innovation" management touts has not yet translated into the bottom-line efficiency of its larger rivals (XBRL).
5. WHAT WOULD CHANGE THIS VIEW?
- Constructive if the Growth Portfolio’s revenue contribution exceeds 60% of total sales, signaling that the transition from legacy drugs is nearing completion.
- Cautious if the "pivotal readouts" expected in the back half of 2026 fail to meet endpoints, as Bristol Myers Squibb lacks the revenue growth to absorb major R&DR&DResearch & Development — spending on creating new products or technologies failures (8-K).
- Cautious if the "maximum fair prices" set under the IRA result in a double-digit percentage decline in Eliquis net realized price, which would impair the cash flow used to service the $37.5 billion debt load (XBRL).
6. BOTTOM LINE
Structural Advantage: A diversified R&DR&DResearch & Development — spending on creating new products or technologies engine spanning CAR-T, protein degraders, and radiopharmaceuticals that provides multiple "shots on goal" to replace aging blockbusters.
Bottom Line: Bristol Myers Squibb is a high-yield value play for investors who believe Bristol Myers Squibb’s new science can outrun its looming patent expirations.
1. Top 5 Material Risks
- Pricing and Reimbursement Controls: Bristol Myers Squibb faces increasing pressure from U.S. and international pricing controls, rebates, and government negotiations. The IRA, in particular, allows the HHS to set prices for single-source drugs, which are expected to represent a significant discount from average prices to wholesalers.
- Loss of Market Exclusivity: The commercial value of Bristol Myers Squibb’s innovative products is concentrated within their exclusivity periods. The emergence of generic or biosimilar competition—often occurring "at risk" before patent expiration—leads to rapid and substantial revenue erosion.
- Pipeline Development and Commercialization: Future success depends on replacing revenue from aging products with new ones. The research and development process carries a high rate of failure, and delays in regulatory approval or commercial launch can negatively impact revenues and earnings.
- Concentration of Revenue: A majority of revenue and earnings is derived from a few key products, specifically Eliquis, Opdivo, Opdivo Qvantig, Orencia, Reblozyl, and Yervoy. Any issue affecting these specific assets, such as patent loss or formulary access changes, poses a material threat to Bristol Myers Squibb’s financial condition.
- Supply Chain and Manufacturing Disruptions: Bristol Myers Squibb is vulnerable to manufacturing shutdowns, quality control failures, and supply chain interruptions. The complexity of producing novel cell-based therapies, such as CAR-T, and radiopharmaceutical therapeutics introduces additional risks of product loss or regulatory remedial action.
2. Company-Specific Risks
- 340B Program Exposure: Bristol Myers Squibb’s policy of limiting the number of designated 340B contract pharmacy locations per hospital has faced legal challenges and scrutiny, and significant changes to these sales or pricing practices could adversely affect profitability.
- Royalty Income Decline: Pretax income is significantly bolstered by royalty streams, which generated approximately $2.7 billion in 2025. These streams are set to decline, with royalties related to Keytruda and Tecentriq terminating on December 31, 2026.
- Debt and Credit Rating: Acquisitions such as Mirati, Karuna, and RayzeBio have increased debt levels, leading to a downgrade of Bristol Myers Squibb’s long-term credit rating by Standard & Poor’s from A+ to A.
- Integration of Acquisitions: Bristol Myers Squibb faces risks related to the successful integration of acquired businesses, including potential impairment charges if the anticipated revenues, profits, or synergies from these assets fail to materialize.
3. Regulatory/Legal Risks
- IRA Compliance: Failure to comply with the IRA’s price-setting process subjects Bristol Myers Squibb to excise taxes and civil monetary penalties.
- Government Agreements: The U.S. Government Agreement requires providing Eliquis for free to Medicaid and donating over seven tons of Eliquis API to the U.S. Strategic Active Ingredient Reserve, which may impact cash flows.
- Environmental and ESG Reporting: Increased focus on ESG disclosures exposes Bristol Myers Squibb to potential liabilities, increased compliance costs, and reputational harm if aspirational goals are not met.
- Forum Selection Bylaws: Bristol Myers Squibb’s bylaws designate the Court of Chancery of the State of Delaware as the exclusive forum for certain lawsuits, which may increase litigation costs for stockholders and discourage legal challenges.
4. Financial Impact Map
IRA Price Setting → Revenue and Profit Margins → HHS-mandated "maximum fair prices" for Eliquis, Pomalyst, and Orencia represent significant discounts from average prices. Loss of Market Exclusivity → Revenue → Rapid and substantial declines in sales following the introduction of generic or biosimilar versions of branded products. Pipeline Failure → Intangible Assets → Potential for material non-cash impairment charges if pipeline programs are canceled or commercial prospects are reduced (e.g., $19.1 billion of other intangible assets as of December 31, 2025). Royalty Stream Termination → Pretax Income → Royalty income, which totaled approximately $2.7 billion in 2025, will decline as specific arrangements for Keytruda and Tecentriq terminate in 2026. Acquisition Debt → Interest Expense → Increased debt from Mirati, Karuna, and RayzeBio acquisitions results in higher interest expense and potential credit rating pressure.
Recent Filings
| Form | Filed | Period |
|---|---|---|
| 10-K | Feb 2026 | Dec 2025 |
| 8-K | Feb 2026 | — |
| 10-Q | Oct 2025 | Sep 2025 |
| 14A | Mar 2025 | — |
AI-extracted key facts from press releases and SEC filings. Significance 1–10.
Bristol-Myers Squibb Phase 3 SCOUT-HCM trial for Camzyos meets primary endpoint in adolescents
- ▸Phase 3 SCOUT-HCM trial met primary endpoint for adolescent HCM patients
- ▸Camzyos showed clinically meaningful Valsalva LVOT gradient reduction versus placebo
- ▸Safety profile in adolescents consistent with adult clinical data
- ▸Company projects $41.3B revenue and $9.2B earnings by 2028
- ▸Expanded Insitro collaboration targets AI-enabled drug discovery for ALS
Bristol Myers Camzyos SCOUT-HCM study meets primary endpoint in adolescent oHCM patients
- ▸SCOUT-HCM study met primary endpoint reducing LVOT gradient in adolescents aged 12-18
- ▸Camzyos 2025 sales exceeded $1 billion, up 77% year over year
- ▸Phase III Librexia ACS study for milvexian discontinued due to efficacy concerns
- ▸Librexia AF and Librexia STROKE studies to continue with data expected 2026
- ▸Cytokinetics received FDA approval for rival drug Myqorzo in December 2025
Merck pursues M&A strategy to diversify pipeline ahead of 2028 Keytruda patent cliff
- ▸Merck executing M&A spree to diversify revenue base
- ▸Acquired Terns Pharmaceuticals assets for $6.7B
- ▸Keytruda exclusivity loss scheduled for 2028
- ▸Strategic focus on pipeline expansion to offset future patent expiration
Bristol Myers Squibb Opdivo Receives FDA and EC Label Expansion for Hodgkin Lymphoma
- ▸FDA approved Opdivo plus AVD for stage III/IV cHL patients 12+ years
- ▸EC approved Opdivo plus brentuximab vedotin for pediatric/young adult relapsed cHL
- ▸Opdivo 2025 global sales reached $10B, up 8% YoY
- ▸Opdualag 2025 sales totaled $1.18B driven by melanoma demand
- ▸Label expansions aim to offset generic revenue erosion from Revlimid and Sprycel
BMY Opdivo Receives FDA and EU Label Expansion for Classical Hodgkin Lymphoma
- ▸FDA approved Opdivo plus AVD for frontline stage III/IV classical Hodgkin lymphoma
- ▸Phase III SWOG 1826 data showed 58% reduction in disease progression or death
- ▸EC approved Opdivo plus brentuximab vedotin for relapsed/refractory pediatric and young adult patients
- ▸Opdivo generated $10 billion in global sales during 2025
- ▸Label expansions broaden addressable market in frontline and relapsed treatment settings
Bristol Myers Squibb expands ALS collaboration with insitro, nominates two new therapeutic targets
- ▸Expanded collaboration adds two new ALS therapeutic targets: ALS-2 and ALS-3
- ▸insitro received $10 million milestone payment for target selection
- ▸Targets identified via insitro’s AI-driven Virtual Human platform
- ▸Collaboration now covers three total ALS targets including initial ALS-1
- ▸Development strategy utilizes multiple modalities including oligonucleotides and small molecules
Bristol Myers Squibb Secures FDA Approval for Sotyktu in Psoriatic Arthritis Treatment
- ▸FDA approved Sotyktu for treatment of adults with active psoriatic arthritis
- ▸Phase 3 SUCCESSOR-2 interim results for oral mezigdomide showed positive data
- ▸Pipeline strategy focuses on oral therapies for immunology and oncology franchises
- ▸Company projects $41.3B revenue and $9.2B earnings by 2028
- ▸New drug launches aim to offset future patent losses on Eliquis and Opdivo
Piper Sandler raises BMY price target to $75 from $66, cites pipeline growth potential
- ▸Piper Sandler raised BMY price target to $75 from $66
- ▸Maintained Overweight rating on BMY shares
- ▸RBC Capital initiated coverage with Sector Perform rating and $60 target
- ▸Analysts cite milvexian efficacy and pipeline progress as growth drivers
- ▸Company faces Eliquis US patent exclusivity loss in 2028