Moderna — Jan 12, 2026 release
Fiscal 2025 fourth-quarter results · 8-K Item 2.02 · Exhibit 99.1 · 0001682852-26-000007
Showing in the filing
GAAP operating expenses
“$5.0 – $5.2 billion (unaudited)”
Period
FY2025
Measure
GAAP-tied
Source
Prose
All guidance in this release · 6
Projected year-end cash balance for FY2025
“approximately $8.1 billion (unaudited)”
Revenue growth target for FY2026
“up to 10%”
GAAP operating expenses for FY2025
“$5.0 – $5.2 billion (unaudited)”
GAAP operating expenses for FY2026
“approximately $4.9 billion”
GAAP operating expenses for FY2027
“$4.2 – $4.6 billion”
Cash breakeven for FY2028
“targeted cash breakeven”
Exhibit 99.1 · the passage around this item
… earlier in the release
Summary of Financial Updates 2025 financial updates: Moderna expects 2025 revenue of approximately $1.9 billion (unaudited), $100 million above the midpoint of the $1.6 – $2.0 billion range communicated on the Company’s 3Q25 Earnings Call. The Company is also improving 2025 expected GAAP operating expenses by $200 million to a range of $5.0 – $5.2 billion (unaudited). Cash, cash equivalents and investments at year-end 2025 were approximately $8.1 billion (unaudited), which includes a $0.6 billion draw down from our recently announced $1.5 billion term loan facility. Full financial details will be reported in connection with the Company’s Earnings Call on February 13, 2026. 2026 financial framework: Moderna reiterates its target of up to 10% revenue growth in 2026. The Company expects GAAP operating expenses of approximately $4.9 billion in 2026. Moderna expects to further reduce GAAP operating expenses to $4.2 – $4.6 billion in 2027, on the path to targeted cash breakeven in 2028. Summary of Late-Stage Pipeline and Approved Product Milestones Seasonal vaccines: • COVID vaccines : Moderna’s new COVID vaccine, mNEXSPIKE®, is currently approved in the U.S., Canada and Australia. Moderna is expecting potential approvals of mNEXSPIKE in Europe, Japan and Taiwan in 2026. • RSV vaccine : Moderna’s RSV vaccine, mRESVIA®, is in an ongoing Phase 3 heterologous revaccination study with data expected in 2026. • Seasonal flu vaccine : The Company has completed submissions for approval of mRNA-1010 in the U.S., Canada, Australia and Europe and expects poten
later in the release …
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other guidance in this release
Text is the filed exhibit, verbatim.