
*These information are as of 07 February 2025.

1. Executive Summary
Key Points
Bristol-Myers Squibb (BMY) is a global biopharmaceutical leader specializing in innovative therapies for oncology, immunology, cardiovascular diseases, and neuroscience. Recent performance highlights include:
- Q4 2024 Revenue: $12.3B (+8% YoY), driven by growth in key products like Eliquis (+11%) and Opdivo (+4%)1515.
- Full-Year 2024 Revenue: $48.3B (+7% YoY), with a GAAP net loss of $(4.41) per share due to acquisition charges.
- 2025 Guidance: Revenue projected at ~$45.5B (down ~6% YoY) due to generic competition, with adjusted EPS of $6.55–$6.85.
Investment Thesis
BMY presents a mixed outlook:
- Strengths: Robust pipeline (10+ new molecular entities by 2030), strategic cost-cutting ($2B savings by 2027), and leadership in oncology.
- Risks: Near-term revenue decline from patent expirations (Revlimid, Eliquis, Opdivo) and high debt ($10B repayment target by mid-2026).
2. Business Overview
What the Company Does
BMY develops and commercializes therapies for serious diseases, with key products:
- Oncology/Hematology: Opdivo (cancer immunotherapy), Revlimid (multiple myeloma).
- Cardiovascular: Eliquis (anticoagulant).
- Neuroscience: Cobenfy (schizophrenia, approved 2024).
Industry Positioning
- Leader in oncology and immunology, ranked among top global pharma companies by revenue.
- Niche player in neuroscience after acquiring Karuna Therapeutics ($14B).
Competitive Landscape
- Major Competitors: Merck, Pfizer, Roche, Johnson & Johnson.
- Differentiation: Strong oncology portfolio (Opdivo), diversified pipeline, and strategic acquisitions (e.g., Karuna, RayzeBio).
3. Financial Analysis
Historical Performance (2020–2024)
Metric | 2020 | 2021 | 2022 | 2023 | 2024 |
Revenue ($B) | 42.5 | 46.4 | 46.2 | 45.0 | 48.3 |
Net Margin (%) | 15.2 | 18.9 | 20.4 | 17.8 | -15.3 |
Operating Cash Flow ($B) | 10.2 | 11.1 | 12.0 | 10.5 | 10.5 |
Key Ratios (2024)
- Profitability: ROE = -16.64%, Net Margin = 17.83%.
- Efficiency: Asset Turnover = 0.39
- Valuation: P/E = -16.64, EV/EBITDA = 21.93
- Leverage: Debt-to-Equity = 2.99
Cash Flow & Dividends
- Generated $10.5B operating cash flow (2024)
- Dividend yield = 4.14%
4. Growth Prospects
Market Opportunities
- Oncology: Expanding Opdivo indications and cell therapies (e.g., Abecma).
- Neuroscience: Cobenfy expected to generate $1B+ annually by 2030.
Management Guidance
- Targeting $45.5B revenue in 2025 (-6% YoY) due to generics impact.
- Prioritizing R&D reinvestment and cost optimization.
Innovation & R&D
- Invested $28B in R&D over 2022–2024
- Pipeline includes 50+ compounds, with 10+ potential approvals by 2030
5. Competitive Advantages (Moats)
Economic Moat Analysis
- IP Portfolio: 30+ major lifecycle management indications in 2025–2030
- Oncology Leadership: Opdivo remains a standard-of-care in melanoma and NSCLC
Sustainability
Moat durability hinges on successful pipeline execution and offsetting ~$10B revenue loss from generics by 2028
6. Risks
Industry-Specific
- Drug pricing reforms (Inflation Reduction Act impact on Eliquis)
- Generic competition for Revlimid, Eliquis, and Opdivo
Company-Specific
- High debt ($10B repayment target by 2026)
- Integration risks from acquisitions (e.g., Karuna)
7. Valuation & Recommendation
Intrinsic Valuation
- DCF model suggests fair value of $464.62[User-provided prior analysis].
Comparative Valuation
Metric | BMY | Industry Avg. |
P/E | -16.64 | 21.0 |
EV/EBITDA | 21.93 | 13.5 |
Uncle’s thinking: Hold. Near-term risks offset long-term pipeline potential.
8. Conclusion
Key Takeaways
- BMY’s growth portfolio (+21% in Q4 2024) shows promise, but generics will pressure revenue through 2025.
- Cost-cutting ($2B by 2027) and pipeline execution are critical.
Actionable Insight
Monitor:
- Cobenfy’s commercial uptake and Phase III trials.
- Progress on debt reduction and margin improvement.
Guiding Principles Applied
- Economic Moat: Strong in oncology but challenged by patent cliffs.
- Valuation Discipline: High EV/EBITDA suggests limited upside.
- Risk Assessment: Diversification needed to mitigate generics impact.