Key takeaways
View moreBMY appears undervalued based on its significantly lower EV/EBITDA multiple (8.57x vs industry average 66.57x) and improving operational metrics, including expanding margins and strong ROE. While the company faces challenges including high debt levels and industry pricing pressures, these risks appear more than priced in given the company's strong market position, promising pipeline, and strategic initiatives for cost savings and growth.
- BMY's profitability is improving, with gross profit margin increasing from 55.74% in Q2 2024 to 65.53% in Q1 2025, driven by effective cost management.
- The company's high financial leverage, with a total debt to total equity ratio of 294.66% in Q1 2025, and potential liquidity concerns, indicated by current and quick ratios below industry averages, warrant close monitoring.
- Inconsistent revenue growth, as evidenced by fluctuating quarterly sales, and high variability in cash flows pose risks to the company's financial stability.
- The strategic productivity initiative, aiming for $2 billion in annual cost savings by 2027, is crucial for improving profitability and providing financial flexibility.
- Recent acquisitions and collaborations, such as the acquisitions of Karuna, RayzeBio, and Mirati, could significantly impact future financial performance and growth potential.
- BMY's Enterprise Value to EBITDA ratio of 8.57 is significantly lower than the industry average of 66.57, suggesting potential undervaluation or concerns about future growth prospects.
- The recent earnings call highlighted the importance of the growth portfolio, with increased full-year revenue guidance to a range of $45.8 billion to $46.8 billion.
- BMY's stock price has fluctuated between $44.12 and $50.69 from April 28, 2025, to June 23, 2025, indicating volatility and sensitivity to market sentiment.
- The company faces significant pricing and market access pressures, particularly in the U.S. and Europe, due to government and payer actions to control drug costs, which is expected to continue impacting revenues and profitability.
- BMY's future hinges on successful pipeline development, cost control, and strategic capital allocation amidst industry headwinds, requiring careful monitoring of pipeline progress and cost management efforts.
Evaluation summary
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Company Overview:
- Bristol Myers Squibb Co. (BMY) is a global biopharmaceutical company engaged in discovering, developing, licensing, manufacturing, marketing, distributing, and selling biopharmaceutical products. Their offerings include small molecules, biologics, and CAR-T cell therapies.
- Key therapeutic areas include oncology, hematology, immunology, cardiovascular, and neuroscience. Major marketed products include Opdivo, Eliquis, Revlimid, Orencia, Yervoy, Reblozyl, Breyanzi, Camzyos, and Cobenfi.
- The company competes with other global research-based biopharmaceutical companies, smaller research companies, and generic drug manufacturers.
- Benchmarks for comparative analysis include the Health Care Select Sector SPDR Fund (XLV), while industry peers include Merck & Co., Inc. (MRK) and GSK Plc (GSK).
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Financial Performance:
- BMY's revenue shows an inconsistent trend. For example, sales/revenue was $11.201 billion for the quarter ending March 31, 2025, compared to $12.342 billion for the quarter ending December 31, 2024.
- Gross profit margin has been increasing, from 55.74% in Q2 2024 to 65.53% in Q1 2025. Net profit margin also improved significantly, from 0.58% in Q4 2024 to 21.93% in Q1 2025.
- Return on Average Assets (ROA) was 5.66% for the quarter ending March 31, 2025, compared to -9.53% for the quarter ending December 31, 2024. Return on Average Total Equity (ROE) was 31.99% for the quarter ending March 31, 2025, compared to -39.10% for the quarter ending December 31, 2024. Return on Average Total Capital (ROTC) was 15.32% for the quarter ending March 31, 2025, compared to 12.90% for the quarter ending December 31, 2024. These are significantly higher than the industry averages of -63.76%, -478.21%, and -134.46%, respectively.
- The recent earnings call indicated increased full-year revenue guidance to a range of $45.8 billion to $46.8 billion, reflecting strong performance of the growth portfolio.
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Operational Efficiency:
- Total current assets increased from $26.89 billion in Q2 2024 to $30.783 billion in Q1 2025. Total current liabilities also increased from $23.265 billion in Q2 2024 to $24.07 billion in Q1 2025.
- Working capital increased from $3.625 billion in Q2 2024 to $6.713 billion in Q1 2025.
- Net operating cash flow decreased from $5.591 billion in Q3 2024 to $1.954 billion in Q1 2025.
- Free cash flow to equity decreased from $5.267 billion in Q3 2024 to $1.694 billion in Q1 2025.
- Total capital expenditure was $260 million in Q1 2025, compared to depreciation, depletion & amortization of $1.012 billion.
- Cash dividends paid were $1.258 billion in Q1 2025.
- The current ratio was 1.28 in Q1 2025, and the quick ratio was 1.17, both below the industry averages of 6.93 and 6.77, respectively.
- The total debt to total equity ratio was 294.66% in Q1 2025.
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Growth Opportunities:
- BMY is focused on maximizing the growth portfolio, accelerating the R&D pipeline, driving operational excellence, and strategically allocating capital.
- The company completed acquisitions of Karuna, RayzeBio, and Mirati in 2024 to expand in neuroscience, oncology, and radiopharmaceuticals.
- They entered a strategic collaboration with SystImmune to co-develop and co-commercialize a bispecific antibody drug conjugate.
- The earnings call highlighted several upcoming catalysts, such as the first look at one of the phase three trials for Cobenfi in Alzheimer's disease psychosis.
- Business development remains a top priority, with the company actively pursuing opportunities that can enhance its growth profile.
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Recent Developments and Market Sentiment:
- The recent earnings call on April 24, 2025, highlighted that BMY's future success hinges on the continued strong performance of its growth portfolio, particularly key drugs like Opdivo, Breyanzi, Reblozyl, and Camzyos.
- The successful launch and adoption of Cobenfi as a foundational monotherapy for schizophrenia is vital for BMY's growth strategy.
- BMY is actively seeking external innovation through business development to strengthen its pipeline and improve its long-term growth profile.
- The company's strategic productivity initiative is crucial for improving profitability and providing financial flexibility for investments in R&D and business development.
- Tariffs, potential changes in US healthcare policy, and global economic uncertainty could impact BMY's financial performance and strategic decisions.
- Upcoming data readouts from key pipeline programs, such as the Cobenfi Alzheimer's disease psychosis trial and the Milvexian trials, will be critical for shaping BMY's future growth prospects.
- The company is focused on US manufacturing and is working to mitigate the impact of potential tariffs.
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Risks and Threats:
- Increased pricing pressure and regulatory restrictions on drug pricing and market access pose a significant risk.
- Potential for earlier-than-expected loss of market exclusivity due to patent challenges and generic/biosimilar competition.
- Difficulties or delays in developing and commercializing new products.
- Reliance on key products like Eliquis, Opdivo, and Revlimid for a significant portion of revenues.
- Exposure to supply chain disruptions, manufacturing issues, and other operational challenges.
- Potential legal and regulatory risks, including from intellectual property disputes, pricing/sales practices litigation, and government investigations.
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Valuation Analysis:
- The Enterprise Value to EBITDA ratio was 8.57 for the quarter ending March 31, 2025, compared to an industry average of 66.57. The Enterprise Value to Sales ratio was 3.44 for the quarter ending March 31, 2025, compared to an industry average of 8681.15.
- Potential catalysts include successful pipeline readouts and positive outcomes from business development initiatives.
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Price Performance:
- BMY's stock price has fluctuated between $44.12 and $50.69 from April 28, 2025, to June 23, 2025.
- Over the past year, BMY outperformed both MRK and GSK, with returns of 16.68% compared to -37.66% for MRK and -2.96% for GSK. However, over longer periods (2 and 3 years), BMY has generally underperformed GSK.
- BMY has shown mixed performance compared to the Health Care Select Sector SPDR Fund (XLV). While BMY outperformed XLV over the past year, it has underperformed over longer periods and year-to-date.
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Future Outlook:
- Management increased full-year revenue guidance to a range of $45.8 billion to $46.8 billion.
- The company is on track to deliver $1 billion of cost savings by the end of this year and $2 billion in annual cost savings by the end of 2027.
- The earnings call highlighted several upcoming catalysts, such as the first look at one of the phase three trials for Cobenfi in Alzheimer's disease psychosis.
- The company expects several opportunities to come this year, such as the first look at one of the phase three trials for Cobenfi in Alzheimer's disease psychosis. Several new pivotal studies are planned, including seven phase three studies for Cobenfi across three indications.
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Summary:
- BMY's strengths include a diversified portfolio of marketed products, a robust pipeline, and a strategic productivity initiative to drive cost savings. Weaknesses include inconsistent revenue growth, high financial leverage, and potential liquidity concerns. Opportunities include market expansion through acquisitions and collaborations, and pipeline advancement in key therapeutic areas. Threats include increased pricing pressure, regulatory restrictions, and potential loss of exclusivity for key products.
- BMY's financial health is mixed, with improving profitability but high debt levels and potential liquidity concerns.
- Critical factors for future performance include successful pipeline development, cost control, and strategic capital allocation.
- Areas requiring further monitoring include revenue consistency, debt levels, and the effectiveness of the productivity initiative.
- BMY presents a mixed investment profile, with growth potential balanced against identified risks. The company's position relative to industry trends and recent developments suggests a need for careful monitoring of pipeline progress and cost management efforts. Potential catalysts include successful pipeline readouts, while headwinds include pricing pressures and regulatory restrictions. Overall, BMY's investment characteristics suggest a higher-risk, higher-reward profile.
Price history
Fundamentals
Insights
- Bristol-Myers Squibb's profitability is improving, driven by effective cost management and increasing gross profit margins.
- The company's high financial leverage and potential liquidity concerns warrant close monitoring.
- Inconsistent revenue growth and high variability in cash flows pose risks to the company's financial stability.
- The strategic productivity initiative and recent acquisitions could significantly impact future financial performance.
- BMS's profitability ratios are significantly higher than the industry average, indicating superior performance.
Analysis
- Revenue
- Revenue is showing an upward trend, but the fit is poor, indicating inconsistent growth.
- The company's sales/revenue is significantly greater than the industry average.
- The company's 3-year and 5-year CAGR show a deceleration in revenue growth.
- Profitability
- Gross profit margin is increasing, driven by decreasing cost of goods sold.
- Operating expenses are trending downward, reflecting cost-cutting measures.
- EBIT and net income are trending upward, indicating improved profitability.
- Profitability ratios (ROA, ROE, ROTC, ROIC) are above average and trending upward, indicating efficient resource utilization.
- Liquidity
- The current and quick ratios are below the industry average, indicating potential liquidity concerns.
- Working capital is increasing, which could improve liquidity.
- Cash and short-term investments are increasing, further improving liquidity.
- Solvency
- The total debt to total equity ratio is high, indicating high financial leverage.
- The debt/EBITDA ratio is below the industry average, suggesting manageable debt levels.
- Long-term debt is increasing, reflecting reliance on debt financing.
- Operational Efficiency
- Accounts receivable are decreasing, suggesting efficient collection or declining sales.
- Inventories are increasing, which could indicate anticipation of higher sales or potential overstocking.
- The company's strategic productivity initiative aims to drive $2 billion in annual cost savings by 2027, which could improve operational efficiency.
- Cash Flow Analysis - Net operating cash flow is trending downward, raising concerns about the sustainability of core business operations. - Free cash flow to equity is trending downward, further indicating potential financial distress. - Cash dividends paid are steadily increasing, indicating a commitment to shareholder returns.
- Risk Factors
- High financial leverage, as indicated by the high total debt to total equity ratio.
- Inconsistent revenue growth, as reflected in the poor fit of the sales/revenue trend.
- Potential liquidity concerns, as indicated by the low current and quick ratios.
- High variability in net income and net operating cash flow, raising concerns about the quality of earnings.
- Future Outlook
- Monitor the trend in equity to ensure long-term solvency.
- Evaluate the effectiveness of the productivity initiative in improving asset utilization and reducing debt.
- Track the impact of acquisitions on intangible assets and overall financial stability.
- Focus on improving revenue consistency and managing debt levels.
- Continue to monitor and manage unusual expenses to understand the true earnings potential.
- Profitability
Financial statements
Public filings
- BMS is a leading global biopharmaceutical company focused on developing innovative medicines across key therapeutic areas, with a diversified portfolio of marketed products and a robust pipeline.
- The company is facing significant pricing and market access pressures, particularly in the U.S. and Europe, due to government and payer actions to control drug costs. This is expected to continue impacting revenues and profitability.
- BMS has been actively expanding its capabilities through strategic acquisitions and collaborations, particularly in areas like neuroscience, oncology, and radiopharmaceuticals. However, integrating these new assets and realizing expected synergies poses execution risks.
- The company's financial performance remains highly dependent on the commercial success of key products like Eliquis, Opdivo, and Revlimid. Loss of exclusivity for these products due to patent challenges and generic/biosimilar competition is a major threat.
- BMS is investing heavily in R&D to advance its pipeline, but faces inherent risks and uncertainties in drug development that could delay or derail promising programs.
- Operational challenges, including supply chain disruptions, manufacturing issues, and legal/regulatory risks, also pose ongoing threats to the business.
- To mitigate these headwinds, BMS is implementing a strategic productivity initiative to drive significant cost savings, which it plans to reinvest in growth areas. Successful execution of this plan will be critical.
Core Business and Operations:
- Bristol-Myers Squibb Company (BMS) is a global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines to help patients prevail over serious diseases
- Key therapeutic areas include oncology, hematology, immunology, cardiovascular, and neuroscience
- Major marketed products include Opdivo, Eliquis, Revlimid, Orencia, Yervoy, Reblozyl, Breyanzi, Camzyos, and Cobenfy
- Sells products globally, with the U.S. and international regions contributing significant revenue
- Competes with other global research-based biopharmaceutical companies, smaller research companies, and generic drug manufacturers
Industry and Market Trends:
- Facing increased pricing pressure and regulatory restrictions on drug pricing and market access in the U.S., EU, and other regions
- Governments and payers are implementing measures to control pharmaceutical costs, including price negotiations, rebates, and limits on reimbursement
- Potential impact from the Inflation Reduction Act (IRA) in the U.S., which allows the government to "negotiate" prices for certain Medicare drugs and requires manufacturers to pay rebates for price increases exceeding inflation
- Ongoing challenges from generic and biosimilar competition eroding revenues for branded products after loss of exclusivity
Recent Events:
- Completed acquisitions of Karuna, RayzeBio, and Mirati in 2024 to expand in neuroscience, oncology, and radiopharmaceuticals
- Entered a strategic collaboration with SystImmune to co-develop and co-commercialize a bispecific antibody drug conjugate
- Achieved multiple regulatory approvals across the portfolio, including for Breyanzi, Reblozyl, Opdivo, Krazati, and Cobenfy
- Implemented a strategic productivity initiative to drive $2 billion in annual cost savings by 2027
Risk Factors:
- Increased pricing pressure and regulatory restrictions on drug pricing and market access
- Potential for earlier-than-expected loss of market exclusivity due to patent challenges and generic/biosimilar competition
- Difficulties or delays in developing and commercializing new products
- Reliance on key products like Eliquis, Opdivo, and Revlimid for a significant portion of revenues
- Exposure to supply chain disruptions, manufacturing issues, and other operational challenges
- Potential legal and regulatory risks, including from intellectual property disputes, pricing/sales practices litigation, and government investigations
Legal Matters:
- Ongoing patent litigation in Europe related to Eliquis, with mixed outcomes across different countries
- Lawsuits related to the labeling, sales, and promotion of Plavix in Hawaii
- Securities litigation matters involving Celgene, including class actions and individual lawsuits related to contingent value rights
- Various antitrust and pricing-related lawsuits involving Thalomid, Revlimid, and Pomalyst
Management's Discussion and Analysis:
- Revenues driven by growth in the company's key marketed products, partially offset by generic erosion in the legacy portfolio
- Profitability impacted by one-time charges related to acquisitions, intangible asset impairments, and higher interest expense
- Investing significantly in R&D to advance the pipeline, with a focus on oncology, hematology, immunology, cardiovascular, and neuroscience
- Maintaining a strong balance sheet and liquidity position to fund operations, dividends, and strategic initiatives
- Executing on a productivity initiative to drive $2 billion in annual cost savings by 2027 to reinvest in growth
Earnings calls
Earnings Report 2025Q1 (2025-04-24)
Key takeaways
- Growth Portfolio is Key: BMY's future success hinges on the continued strong performance of its growth portfolio, particularly key drugs like Opdivo, Breyanzi, Reblozyl, and Camzyos.
- Cobenfi's Launch is Critical: Despite the mixed clinical trial results, the successful launch and adoption of Cobenfi as a foundational monotherapy for schizophrenia is vital for BMY's growth strategy.
- Business Development is a Priority: BMY is actively seeking external innovation through business development to strengthen its pipeline and improve its long-term growth profile.
- Cost Management is Essential: The company's strategic productivity initiative is crucial for improving profitability and providing financial flexibility for investments in R&D and business development.
- External Factors Pose Risks: Tariffs, potential changes in US healthcare policy, and global economic uncertainty could impact BMY's financial performance and strategic decisions.
- Pipeline Readouts are Important: Upcoming data readouts from key pipeline programs, such as the Cobenfi Alzheimer's disease psychosis trial and the Milvexian trials, will be critical for shaping BMY's future growth prospects.
- Focus on US Manufacturing: The company is focused on US manufacturing and is working to mitigate the impact of potential tariffs.
Focus of management’s prepared remarks
- Growth Portfolio Performance: The growth portfolio delivered double-digit sales growth, driven by key marketed products like the IO portfolio, Breyanzi, Reblozyl, and Camzyos.
- Recent Launches: Cobenfi, a novel schizophrenia treatment, and Opdivo Cuvanti, the subcutaneous formulation of nivolumab, are receiving positive early feedback.
- Pipeline Advancement: Opdivo plus Yervoy received FDA and EMA approvals for liver cancer and FDA approval for MSI high colorectal cancer. Breyanzi was approved in the EU for follicular lymphoma. Camzyos received approval in Japan and a favorable label update in the US. Milvexian completed enrollment in the Librexia atrial fibrillation trial.
- Clinical Trial Results: The Camzyos Odyssey study in non-obstructive HCM and the Cobenfi Arise study in adjunctive schizophrenia did not meet their primary endpoints, but these outcomes are not expected to significantly impact the company's strategy or growth trajectory.
- Upcoming Catalysts: The company expects several opportunities to come this year, such as the first look at one of the phase three trials for Cobenfi in Alzheimer's disease psychosis. Several new pivotal studies are planned, including seven phase three studies for Cobenfi across three indications.
- Business Development: Business development remains a top priority, with the company actively pursuing opportunities that can enhance its growth profile.
- Operational Excellence: The company is taking deliberate actions to rightsize its cost structure and become a more efficient company. The strategic productivity initiative is expected to realize approximately $2 billion in annual cost savings by the end of 2027.
- Global Operating Climate: The company is focused on building a strong and resilient company that can navigate and manage through operating complexities.
- Financial Outlook: Increased full-year revenue guidance to a range of $45.8 billion to $46.8 billion, reflecting strong performance of the growth portfolio, better-than-expected legacy sales in the first quarter, and a favorable impact of approximately $500 million related to foreign exchange rates.
Focus of the analyst Q&A
- Impact of Tariffs:
- The company's US manufacturing footprint and ability to shift manufacturing to the US over time.
- Flexibility of transfer pricing assumptions and ability to step up inventory as a potential strategy.
- Cobenfi Outlook:
- Impact of the adjunctive trial results on the outlook for Cobenfi.
- Use of Cobenfi in adjunctive settings given the negative trial results.
- R&D Strategy:
- Changes in the thought process regarding taking bets in R&D.
- Future pipeline and riskiness of it.
- Cobenfi in Alzheimer's Psychosis:
- Impact of the ARISE readout on confidence in the Alzheimer's psychosis readout.
- Additional trials that may be planned.
- Business Development Strategy:
- Factors influencing the company's strategy and urgency regarding business development.
- Impact of recent deals for Chinese assets and low valuations across US SMID biotech.
- Most Favored Nation Pricing:
- Potential implementation of most favored nation's pricing and its impact on negotiations for IRA drug prices.
- Camzyos Sales Acceleration:
- Potential positive impact on relaxed cardiac monitoring for Camzyos and how this could help accelerate sales.
- Cobenfi Prescriber Base:
- Details on the prescriber base for Cobenfi, in terms of breadth and depth.
- Cadence of gross-to-net over the course of the year.
- 2026 Operating Margin:
- Directional outlook for the 2026 operating margin.
- Camzyos Alzheimer's Psychosis Trial:
- Expectations for the bar for the Alzheimer's psychosis trial.
- Meaningful reduction in hallucinations and delusions.
- Capital Investments in the US:
- Comments on Bristol's perspective on committed capital expenditure in the US going forward.
- Long-Term Guidance:
- Expectations to revisit long-term guidance at some point.
- Assurance that the trough number won't go lower than $6 a share.
- Engagement with Washington:
- How Bristol's leadership team and board are engaging differently with Washington to defend the industry and company.
- Milvexian Phase III Trial:
- Extent to which the Milvexian Phase III trial benefited from the competitor Phase III stoppage.
- Camzyos Defensibility:
- How defensible is the first-in-class position with Camzyos in light of potential competition.
- Radio Ligand Franchise:
- Expectations from RACE101 in first-line small cell lung cancer.
- FDA Changes:
- Potential impact of the FDA commissioner's vision for changes at the FDA.
- PD-1 VEGF Datasets:
- Thoughts on the recent PD-1 VEGF datasets.
Summary
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Financial Performance
Bristol-Myers Squibb (BMY) reported a strong Q1 2025, exceeding expectations and leading to increased full-year guidance. Total company revenues were approximately $11.2 billion. Diluted earnings per share were $1.80. The company increased its full-year revenue guidance to a range of $45.8 billion to $46.8 billion and raised the midpoint 2025 non-GAAP EPS guidance by 15¢ per share, with an expected range between $6.70 and $7.
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Revenue Drivers
Revenue growth was primarily driven by the growth portfolio, which increased approximately 18%, led by key brands, including the IO portfolio, Breyanzi, Reblozyl, and Camzyos. Cobenfi, the newly launched schizophrenia treatment, contributed $27 million in sales. The legacy portfolio performance primarily reflected the impact of generic entries for certain older brands and Medicare Part D redesign. Revlimid sales were stronger than anticipated.
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Profit Margins and Cost Management
Gross margin was approximately 73%, primarily due to product mix. Operating expenses were more than $500 million lower compared to the same period last year, primarily reflecting the results of the strategic productivity initiative. The company is on track to deliver $1 billion of cost savings by the end of this year and $2 billion in annual cost savings by the end of 2027. The operating margin target of approximately 37% for the full year remains unchanged.
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Guidance and Outlook
The company increased its full-year revenue guidance to a range of $45.8 billion to $46.8 billion. The legacy portfolio is now expected to decline approximately 16% to 18% for the year, a more moderate rate than previously anticipated. Full-year sales of Revlimid are projected to be at the top end of the previously guided range, $2 billion to $2.5 billion. The full-year tax rate guidance remains at 18%. The revised guidance includes the estimated impact of current tariffs on US products shipped to China but does not account for any potential pharmaceutical sector tariffs.
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Strategic Initiatives
Key strategic initiatives include maximizing the growth portfolio, accelerating the R&D pipeline, driving operational excellence, and strategically allocating capital. Business development remains a top priority. The company is actively pursuing opportunities that can enhance its growth profile. The company is also focused on rightsizing its cost structure and becoming a more efficient company.
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Management Commentary
Management expressed confidence in the company's ability to deliver on disciplined execution and position the company for top-tier growth by the end of the decade. They emphasized the strength of the portfolio, the breadth of opportunities in the pipeline, and the company's ability to navigate and manage through operating complexities. Management highlighted the company's commitment to innovating for patients and strategically allocating capital. The CEO stated that the recent study results for Camzyos and Cobenfi do not meaningfully alter the company's strategy or growth trajectory.
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Industry and Market Conditions
Management acknowledged the uncertainty in the current global operating climate, including potential tariffs, a potential economic downturn, and restructuring at the FDA and HHS. They also addressed concerns about potential implementation of most favored nation's pricing and its impact on negotiations for IRA drug prices. The company is focused on strengthening the ecosystem for innovation in the US and engaging with the government on pricing and the support of the payment for innovation.
Comparative analysis
Benchmarks (as of 2025-06-23)
- Performance Comparison:
- Bristol Myers Squibb Co. (BMY) has shown mixed performance compared to the Health Care Select Sector SPDR Fund (XLV). Over the past year, BMY outperformed XLV with a return of 16.68% compared to -8.34%. However, over longer periods such as 2 and 3 years, BMY underperformed XLV, with returns of -20.76% and -33.82% respectively, compared to XLV's 4.06% and 7.03%. Year-to-date, BMY has also underperformed XLV, with returns of -15.56% and -3.13% respectively.
- Risk and Return Analysis:
- The annualized returns show that BMY has a higher return over the past year (16.68%) compared to XLV (-8.34%). However, over 2 and 3 years, BMY's annualized returns are -10.98% and -12.85% respectively, while XLV's are 2.01% and 2.29% respectively, indicating underperformance.
- BMY's annualized volatility has been generally higher than XLV's, indicating that BMY is more volatile. For example, in Q2 2024, BMY's volatility reached 44.8% while XLV's was 15.72%.
- BMY's maximum drawdown was -47.67% on 2024-07-03, significantly larger than XLV's maximum drawdown of -17.11% on 2025-05-14. This indicates that BMY has a higher risk profile due to the potential for larger declines from peak values.
- Risk-Adjusted Performance:
- BMY's Sharpe Ratios are generally lower and frequently negative compared to XLV, indicating lower risk-adjusted returns. For example, as of Q2 2025, BMY's Sharpe ratio is 0.67 while XLV's Sharpe ratio is -0.45.
- BMY's beta values are consistently below 1, indicating that it is less sensitive to market movements than XLV. As of Q2 2025, BMY's beta is 0.24 while XLV's beta is 0.47.
- Overall Assessment:
- Bristol Myers Squibb Co. (BMY) has shown mixed performance compared to the Health Care Select Sector SPDR Fund (XLV). While BMY outperformed XLV over the past year, it has underperformed over longer periods and year-to-date. BMY is also more volatile and has a higher risk profile due to its larger maximum drawdown. The Sharpe Ratios indicate that XLV generally offers better risk-adjusted returns. BMY's lower beta suggests it is less sensitive to market movements, which may appeal to risk-averse investors, but it also means it may not benefit as much from market upturns.
Peers Price History(as of 2025-06-23)
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Performance Comparison:
- Bristol Myers Squibb Co. (BMY) has shown mixed performance compared to Merck & Co., Inc. (MRK) and GSK Plc (GSK). Over the past year, BMY outperformed both MRK and GSK, with returns of 16.68% compared to -37.66% for MRK and -2.96% for GSK. However, over longer periods (2 and 3 years), BMY has generally underperformed GSK. For example, over the last three years, BMY's return was -33.82%, while MRK's was -7.31% and GSK's was -4.28%.
- The consistency of BMY's performance has varied. While it showed strong outperformance over the last year, its longer-term performance has been less impressive, indicating periods of underperformance relative to its peers.
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Risk and Return Analysis:
- The annualized returns show that BMY provided a higher return than both MRK and GSK over the past year (16.68% vs. -37.66% and -2.96%, respectively). However, over 2 and 3 years, BMY's annualized returns were negative and lower than MRK's.
- In terms of annualized volatility, BMY's volatility has fluctuated. In Q2 2024, BMY reached a high volatility of 44.8%, while MRK reached 44.64% and GSK reached 43.03%.
- The maximum drawdown for BMY was -47.67% on 07/03/2024, which is larger than the maximum drawdown for MRK (-43.44% on 05/14/2025) and GSK (-40.46% on 09/26/2022). This indicates a higher risk profile for BMY.
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Risk-Adjusted Performance:
- The Sharpe Ratio for BMY was generally lower than that of MRK for most of the period, indicating that MRK offered better risk-adjusted returns. However, there were periods where BMY's Sharpe Ratio surpassed MRK's, suggesting temporary outperformance on a risk-adjusted basis.
- BMY's beta values were generally below 1, indicating that the stock was less volatile than the overall market. However, BMY's increasing beta in late 2023 and early 2024 suggests a slightly higher sensitivity to market movements.
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Overall Assessment:
- Bristol Myers Squibb Co. (BMY) has demonstrated mixed performance compared to Merck & Co., Inc. (MRK) and GSK Plc (GSK). While BMY has shown strong outperformance over the past year, its longer-term performance has been less consistent. BMY's higher maximum drawdown and fluctuating Sharpe Ratio indicate a higher risk profile compared to its peers.
- Recent trends show that BMY experienced high volatility and a significant drawdown in Q2 2024. The increasing beta in late 2023 and early 2024 suggests a higher sensitivity to market movements. These factors should be carefully considered when evaluating BMY as an investment.
Peers Fundamentals(as of 2025-03-31)
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Market Position and Size:
- Bristol Myers Squibb (BMY) holds a mid-range market position compared to its peers. Its market capitalization of $95,485.95 million is significantly less than Merck & Co., Inc. (MRK) at $201,284.16 million but greater than GSK Plc (GSK) at $56,800.03 million.
- BMY's revenue ($47,636 million) and EBITDA ($18,948 million) also fall between those of MRK and GSK, indicating a substantial but not dominant presence in the "Pharmaceuticals: Major" industry.
- BMY's net income of $5,419 million is less than MRK's $17,434 million but greater than GSK's $3,153 million.
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Profitability and Efficiency:
- BMY's profitability metrics, including Gross Profit Margin (59.16%), EBITDA Margin (39.78%), and Net Profit Margin (11.38%), are generally lower than MRK's but higher than GSK's.
- Compared to the industry average, BMY's profitability metrics are significantly better, as the industry average is a negative number.
- BMY's efficiency in generating returns, as measured by Return on Average Assets (5.66%), Return on Average Total Equity (31.99%), and Return on Average Total Capital (15.32%), is moderate compared to its peers.
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Financial Health and Stability:
- BMY's liquidity, as indicated by its Current Ratio (1.28) and Quick Ratio (1.17), is moderate compared to its peers and below the industry average.
- BMY's Total Debt to Total Equity Ratio (294.66) is significantly higher than MRK (72.09) and GSK (130.2), indicating a more leveraged financial position.
- BMY's Debt / EBITDA ratio is 2.62, which is greater than MRK (1.31) and GSK (2.05), but less than the industry average of 6.2.
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Valuation and Market Perception:
- BMY's valuation metrics, including Enterprise Value To Sales (3.44), Enterprise Value To EBITDA (8.57), and Price To Earnings (17.62), suggest it is reasonably valued compared to its peers.
- BMY's Price to Book Ratio (5.49) is greater than MRK (4.17) and GSK (4.05), indicating a higher valuation of its assets.
- BMY's Price To Sales Ratio (2.01) is less than MRK (3.18) but greater than GSK (1.84).
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Cash Flow and Capital Management:
- BMY's Net Operating Cash Flow ($14,310 million) and Free Cash Flow ($13,086 million) are substantial, indicating strong cash generation capabilities.
- BMY's Total Capital Expenditure ($1,224 million) is less than MRK ($3,839 million) and GSK ($2,867 million), suggesting a more conservative approach to capital investments.
- BMY's Cash Flow / Total Debt is 30.39, which is less than MRK (71.39) and GSK (35.28).
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Growth and Future Prospect:
- BMY's 5-Year CAGR in Sales/Revenue (8.97%) is greater than its peers and the peer average, indicating strong long-term revenue growth.
- BMY's net income and basic earnings per share growth have been highly volatile and generally underperforming compared to peers.
- BMY's most recent year-over-year growth rates for Sales/Revenue, EBITDA, and Free Cash Flow are lower than their respective 5-year CAGRs, indicating a deceleration in growth.
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Potential for Investment:
- BMY presents a mixed investment profile. Its strong revenue growth and reasonable valuation metrics are attractive.
- However, its high debt levels, lower profitability compared to MRK, and inconsistent earnings growth raise concerns.
- Investors should carefully weigh these factors and consider BMY's growth potential and financial stability relative to its peers before making an investment decision.
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Key Risks and Considerations:
- BMY's high debt levels pose a significant risk, as they increase financial leverage and vulnerability to economic downturns.
- The volatility in BMY's net income and basic earnings per share growth raises concerns about the sustainability of its overall growth profile.
- BMY's lower profitability compared to MRK suggests potential inefficiencies or higher costs that need to be addressed.
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Overall Assessment:
- BMY's overall financial health is moderate compared to its peers. It exhibits strong revenue growth and cash flow generation, but its high debt levels and lower efficiency in asset utilization raise concerns.
- While BMY outperforms GSK in several metrics, it generally underperforms MRK, indicating room for improvement in operational efficiency and financial management.
- BMY occupies a mid-tier position within its peer group, suggesting it is a significant player in the "Pharmaceuticals: Major" industry but not a dominant leader.