Moderna — Jul 31, 2026 release
Fiscal 2026 second-quarter results · 8-K Item 2.02 · Exhibit 99.1 · 0001682852-26-000147
Showing in the filing
Income Taxes
“negligible”
Period
FY2026
Measure
Company-defined measure
Source
Guidance table
All guidance in this release · 12
Revenue growth for FY2026
“up to 10% growth from 2025 revenue”
Revenue split for FY2026
“approximately 50% U.S. and approximately 50% international”
Revenue split - international for FY2026
“approximately 50%”
Second half 2026 revenue recognized for Q3 FY2026
“approximately 55%”
Share of second half 2026 revenue recognized… for Q3 FY2026
“approximately 55%”
Cost of sales for FY2026
“approximately $1.7 billion”
Research and development expenses for FY2026
“approximately $2.9 billion”
Selling, general and administrative expenses for FY2026
“approximately $1.0 billion”
Income Taxes for FY2026
“negligible”
Tax expense for FY2026
“negligible”
Capital expenditures for FY2026
“$0.2 to $0.3 billion”
Year-end cash and investments for FY2026
“$4.7 to $5.2 billion”
Exhibit 99.1 · the passage around this item
… earlier in the release
Research and Development Expenses: Research and development expenses for 2026 are now anticipated to be approximately $2.9 billion, lowered from approximately $3.0 billion. Selling, General and Administrative Expenses: Selling, general and administrative expenses for 2026 are projected to be approximately $1.0 billion. 2 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 $4.7 to $5.2 billion, an improvement of approximately $0.2 billion. This 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 has received European Commission marketing authorization for mCOMBRIAX in the EU and its mRNA-1083 regulatory filings are under review in Japan, Canada and Australia. The Company is awaiting further guidance from the U.S. FDA on refiling the submission for its flu plus COVID combination vaccine. • Seasonal flu vaccine : The Company's mRNA-1010 regulatory filings are under review in Europe, Canada and Australia and potential approvals are expected to begin in 2026. The U.S. FDA has assigned a PDUFA date for mRNA-1010 of August 5, 2026. • Norovirus vaccine : Moderna's Phase 3 safety and efficacy study of mRNA-1403 did not meet statistical criteria for early success at the Phase 3 interim analysis. Th
later in the release …
the item shown at left
other guidance in this release
Text is the filed exhibit, verbatim.