HighGravityData
Companies / Moderna / Filing

Moderna — Jan 12, 2026 release

Fiscal 2025 fourth-quarter results · 8-K Item 2.02 · Exhibit 99.1 · 0001682852-26-000007
Open on SEC.gov ↗
Showing in the filing
Cash breakeven
“targeted cash breakeven”
Period
FY2028
Measure
Company-defined measure
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
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 potential approvals to begin in 2026. • Seasonal flu/COVID vaccine : The Company's mRNA-1083 filing is under review with the European Medicines Agency (EMA). Moderna submitted for approval to Health Canada in 2025. The Company is awaiting further guidance from the U.S. FDA on refiling. • Norovirus vaccine : Moderna’s ongoing Phase 3 study of mRNA-1403 is enrolling a second Northern Hemisphere season (2025-2026) for additional case accruals, which will inform the timing of the Phase 3 readout. The Company expects an interim analysis in 2026. Oncology therapeutics: • Intismeran autogene : The Company is advancing mRN
later in the release …
the item shown at left
other guidance in this release
Text is the filed exhibit, verbatim.