Bristol-Myers Squibb 8-K
EarningsGuidance loweredImpairment / charge
Growth Portfolio momentum lifts FY2026 revenue outlook to ≈$49.75B-$50.25B; acquired IPRD weighs on non-GAAP EPS outlook, cut to $6.35-$6.55.
Filed 2026-10-29 07:05 ET
- 2.02 Results of Operations
- 7.01 Regulation FD Disclosure
- 9.01 Financial Statements and Exhibits
Summary
Bristol Myers Squibb reported Q3 2026 results and raised its FY2026 revenue outlook while lowering its non-GAAP EPS outlook. Growth Portfolio revenue rose 12%, offsetting expected generic pressure on mature products; the company attributed the updated outlook primarily to continuing portfolio momentum.
Key Figures
| Metric | Q3 2026 | 9M 2026 |
|---|---|---|
| Revenue | $13.1B, +7% Y/Y | $37.5B, +5% Y/Y |
| Gross margin, GAAP | 68.3%, vs 71.9% | 69.9%, vs 72.4% |
| Gross margin, non-GAAP | 68.4%, vs 72.9% | 70.0%, vs 72.9% |
| Net earnings attributable to BMS, GAAP | $2.16B, -2% Y/Y | $8.16B, +37% Y/Y |
| Net earnings attributable to BMS, non-GAAP | $2.77B, -17% Y/Y | $10.2B, +2% Y/Y |
| Diluted EPS, GAAP | $1.05, -3% Y/Y | $3.98, +36% Y/Y |
| Diluted EPS, non-GAAP | $1.35, -17% Y/Y | $4.97, +2% Y/Y |
| Operating cash flow | $4.2B, vs $6.3B | — |
- Growth Portfolio revenue was $7.66B, +12% Y/Y; Legacy Portfolio revenue was $5.42B, +1%. Total U.S. revenue rose 9% to $9.07B, while international revenue increased 3% to $4.00B (4% excluding foreign exchange).
- Growth was led by Eliquis ($4.69B, +25%), Breyanzi ($526M, +46%), Reblozyl ($750M, +22%), Camzyos ($420M, +42%) and Opdualag ($367M, +23%). Opdivo revenue fell 6% to $2.37B; generic competition drove declines in Revlimid (-47%) and Pomalyst/Imnovid (-81%).
- GAAP and non-GAAP diluted EPS included a $(0.58) per-share net impact from acquired in-process research and development charges and licensing income. Lower gross margins reflected product mix and, to a lesser extent, a one-time contract termination charge.
- At 9/30/2026, cash, cash equivalents and marketable debt securities totaled $13.0B, total debt was $42.9B and net debt was $29.9B. The company had approximately $5B of share repurchase authorization remaining.
Guidance
| Metric | Period | Guidance | Prior | Direction |
|---|---|---|---|---|
| Total revenues, non-GAAP guidance (reported and excluding foreign exchange) | FY2026 | ≈$49.75B-$50.25B | ≈$49.0B-$50.0B, July 2026 | Raised |
| Gross margin, non-GAAP | FY2026 | ≈69%-70% | Unchanged, July 2026 | Reaffirmed |
| Operating expenses, non-GAAP | FY2026 | ≈$16.5B | Unchanged, July 2026 | Reaffirmed |
| Other income/(expense), non-GAAP | FY2026 | ≈$(650)M expense | ≈$(700)M, July 2026 | Lowered expense |
| Effective tax rate, non-GAAP | FY2026 | ≈18% | Unchanged, July 2026 | Reaffirmed |
| Diluted EPS, non-GAAP | FY2026 | $6.35-$6.55 | $6.75-$7.00, July 2026 | Lowered |
| Acquired IPRD and licensing income impact on diluted EPS | FY2026 | $(0.60) | $(0.02), July 2026 | Increased deduction |
| Legacy Portfolio revenue | FY2026 | 3%-5% decline | — | — |
| Worldwide Eliquis revenue growth | FY2026 | 20%-25% vs 2025 | Unchanged, July 2026 | Reaffirmed |
Guidance changes, derived from earlier filings
| Metric | Period | Earlier guidance | Guidance now | Change |
|---|---|---|---|---|
| Total revenues, non-GAAP guidance (reported and excluding foreign exchange) | FY2026 | ≈$49.0B-$50.0B | ≈$49.75B-$50.25B | raised |
| Gross margin, non-GAAP | FY2026 | ≈69%-70% | ≈69%-70% | reaffirmed |
| Operating expenses, non-GAAP | FY2026 | ≈$16.5B | ≈$16.5B | reaffirmed |
| Other income/(expense), non-GAAP | FY2026 | ≈$(700)M | ≈$(650)M expense | raised |
| Effective tax rate, non-GAAP | FY2026 | ≈18% | ≈18% | reaffirmed |
| Diluted EPS, non-GAAP | FY2026 | $6.75-$7.00 | $6.35-$6.55 | lowered |
| Legacy Portfolio revenue | FY2026 | 4%-6% decline | 3%-5% decline | raised |
| Worldwide Eliquis revenue growth | FY2026 | 20%-25% | 20%-25% vs 2025 | reaffirmed |
Investor Takeaways
- Track FY2026 revenue against the raised $49.75B-$50.25B range and non-GAAP EPS against $6.35-$6.55; the outlook pairs continued portfolio momentum with a projected Legacy Portfolio decline.
- Watch whether Growth Portfolio revenue sustains its Q3 12% Y/Y growth, supported by demand for medicines including Breyanzi and Camzyos, as generic pressure continues on older products.
- Upcoming pipeline evidence includes Zenbexus Phase 3 relapsed/refractory multiple myeloma data and golcadomide Phase 2 data at ASH; the company also lists a 5/13/2027 FDA decision date for mezigdomide.
The summary is written by an AI model reading the filing.
Model 005 · prompt v111 · 2026-10-29 14:34:04Z