Moderna — May 1, 2026 release
Fiscal 2026 first-quarter results · 8-K Item 2.02 · Exhibit 99.1 · 0001682852-26-000057
Showing in the filing
Selling, general and administrative expenses
“approximately $1.0 billion”
Period
FY2026
Measure
GAAP-tied
Source
Prose
All guidance in this release · 12
Litigation settlement payment for Q3 FY2026
“$950 million”
Revenue growth for FY2026
“up to 10% growth from 2025 revenue”
Revenue geographic split for FY2026
“approximately 50% U.S. and approximately 50% international”
Revenue split - International for FY2026
“approximately 50%”
Revenue split - U.S. for FY2026
“approximately 50%”
Cost of sales for FY2026
“approximately $1.8 billion, including the $0.9 billion non-recurring litigation settlement charge”
Research and development expenses for FY2026
“approximately $3.0 billion”
Selling, general and administrative expenses for FY2026
“approximately $1.0 billion”
Income Taxes for FY2026
“full-year tax expense to be negligible”
Tax expense for FY2026
“negligible”
Capital expenditures for FY2026
“$0.2 to $0.3 billion”
Year-end cash and investments for FY2026
“$4.5 to $5.0 billion”
Exhibit 99.1 · the passage around this item
… earlier in the release
2 Research and Development Expenses: Research and development expenses for 2026 are anticipated to be approximately $3.0 billion. Selling, General and Administrative Expenses: Selling, general and administrative expenses for 2026 are projected to be approximately $1.0 billion. Income Taxes: The Company expects its full-year tax expense to be negligible. Capital Expenditures: Capital expenditures for 2026 are expected to be $0.2 to $0.3 billion. Cash and Investments: Year-end cash and investments for 2026 are now projected to be $4.5 to $5.0 billion, which excludes any further drawdowns from the Company's remaining $0.9 billion available under its credit facility. Recent Progress and Upcoming Late-Stage Pipeline Milestones Infectious disease vaccines: • Seasonal flu + COVID vaccine : Moderna recently presented mRNA-1083 data from a Japanese cohort at the 2026 European Society of Clinical Microbiology and Infectious Diseases (ESCMID) Global Congress. The Company has received European Commission marketing authorization for mCOMBRIAX in the EU and its mRNA-1083 regulatory filings are under review in Canada and Australia. Moderna is awaiting further guidance from the U.S. FDA on refiling the submission for its flu plus COVID combination vaccine. • Seasonal flu vaccine : Moderna recently presented mRNA-1010 revaccination data at the 2026 ESCMID Global Congress. The Company's mRNA-1010 regulatory filings are under review in Europe, Canada and Australia and po
later in the release …
the item shown at left
other guidance in this release
Text is the filed exhibit, verbatim.