Moderna 8-K
PositiveEarningsGuidance raised
Higher international COVID vaccine sales under government partnerships lift FY2026 revenue growth guidance to 15%-25%.
Filed 2026-11-06 06:47 ET
- 2.02 Results of Operations
- 9.01 Financial Statements and Exhibits
Summary
Q3 2026 results with updated FY2026 guidance. Higher international COVID vaccine sales under long-term government partnerships drove revenue to $1.31B, up 29% Y/Y; revenue growth accelerated to +805.5% Q/Q from -62.7% Q/Q in Q2.
FY2026 revenue growth guidance was raised to 15%-25% from up to 10%, and year-end cash and investments guidance was raised to $8.1B-$8.3B from $4.7B-$5.2B.
Developments
- U.S. approval of mFLUSIVA, Moderna’s seasonal influenza vaccine, covers adults 50–64 and accelerated approval covers adults 65 and older. A limited U.S. launch is planned for the 2026–2027 season because approval came after annual contracting; Canada also approved the vaccine.
- Phase 3 results for intismeran autogene, an investigational oncology therapy, in resected high-risk melanoma showed a 42% lower risk of recurrence or death and a 38% lower risk of distant metastasis or death with KEYTRUDA versus KEYTRUDA alone. Moderna and Merck are preparing regulatory submissions and a potential launch, subject to approval.
- A five-year agreement with a local manufacturer in Mexico for COVID vaccines supports international expansion and recurring revenue.
- The registrational study of Moderna’s propionic acidemia treatment reached target enrollment, with pivotal data expected in 2026.
Results with guidance
| Metric | Q3 2026 actual | 9M 2026 | FY2026 guide |
|---|---|---|---|
| Revenue | $1.31B+29% Y/Y, +806% Q/Q | $1.85B+46% Y/Y | 15%-25% growth Y/Yraised from up to 10% |
| Cash and marketable securities | $8.00B+16% Q/Q | — | $8.1B-$8.3Braised from $4.7B-$5.2B |
| Cost of sales | — | — | $1.7Breaffirmed from $1.7B |
| Capital expenditures | — | $146M-4.6% Y/Y | $200Mnarrowed from $200M-$300M |
| GAAP operating expense outlook improvement | — | — | $200Mreaffirmed from $200M |
| Non-recurring litigation settlement charge | — | — | $900Mreaffirmed from $900M |
| Research and development expenses | — | — | $2.7Blowered from $2.9B |
| Selling, general and administrative expenses | — | — | $1Breaffirmed from $1B |
Results without guidance
| Metric | Q3 2026 | Change | 9M 2026 |
|---|---|---|---|
| Operating income | $130M | vs -$260M Y/Y, vs -$815M Q/Q | -$2.07Bvs -$2.22B Y/Y |
| Net income | $162M | vs -$200M Y/Y, vs -$782M Q/Q | -$1.96Bvs -$2.00B Y/Y |
| Diluted EPS | $0.38 | vs -$0.51 Y/Y, vs -$1.97 Q/Q | -$4.93vs -$5.15 Y/Y |
| Cash and cash equivalents | $1.20B | -31% Q/Q | — |
| Diluted shares | 430M | +10% Y/Y, +8.0% Q/Q | 398M+2.6% Y/Y |
What moved the numbers
- Revenue mix: $780M in the U.S. and $533M internationally. Cost of sales was $318M, including $65M of third-party royalties, up 54% Y/Y on higher sales volume and manufacturing-related costs.
- Research and development expense was $583M, down 27% Y/Y as certain late-stage infectious-disease studies wound down and the company continued cost efficiencies. Selling, general and administrative expense was $282M, up 5% Y/Y.
- The $3.0B principal amount of convertible senior notes generated $2.6B in net proceeds after $329M for capped calls and $43M in issuance costs; proceeds support oncology investment and future debt obligations. The principal amount was ≈44% of Moderna’s $6.84B stockholders’ equity at 9/30/2026.
- Net cash used in operating activities was $2.72B for 9M 2026. Accounts receivable increased $1.18B, with much of third-quarter product sales still uncollected at quarter-end; the company also cited seasonal working-capital effects.
Figures extracted from the filings and checked against their text; changes and verdicts computed from them.
The summary is written by an AI model reading the filing.
Model 005 · prompt v189 · 2026-11-06 15:59:59Z