Moderna 8-K

EarningsGuidance loweredImpairment / charge

Norovirus vaccine misses Phase 3 interim early-success criteria, with another cohort planned; cost and R&D outlook lowered.

Filed 2026-07-31 07:03 ET

Summary

Q2 2026 results and updated 2026 financial outlook. Revenue was nearly flat Y/Y, while net loss narrowed; Moderna lowered its cost of sales and R&D outlook and improved its year-end cash projection. Its norovirus vaccine candidate did not meet the Phase 3 interim criteria for early success, and the trial continues with an additional cohort planned.

Key Figures

Metric Q2 2026 Q2 2025 Y/Y
Revenue $145M $142M +2.1%
Operating loss $(815)M $(907)M 10% narrower
Net loss $(782)M $(825)M 5% narrower
Diluted EPS $(1.97) $(2.13) 7.5% narrower
  • Revenue growth reflected UK deliveries under a government partnership and higher stand-ready manufacturing and collaboration revenue, offsetting lower COVID vaccine sales in the U.S. and South America. Cost of sales was $93M, down 22% Y/Y, including $41M of inventory write-downs; R&D was $651M, down 7%, and selling, general and administrative expense was $216M, down 6%.
  • For H1 2026, net loss was $(2.13)B vs $(1.80)B in H1 2025; operating cash flow was $(1.16)B vs $(1.96)B. Cash, cash equivalents and investments were $6.9B at 6/30/2026, down from $7.5B at 3/31/2026, primarily reflecting operating cash use and R&D investment. Moderna paid $950M in July for its previously announced litigation settlement.

Guidance

Metric Period Guidance Prior Direction
Revenue growth FY2026 Up to 10% Y/Y — Reaffirmed
Revenue by geography FY2026 ≈50% U.S.; ≈50% international — —
Revenue recognition Q3 2026 ≈55% of H2 2026 revenue — —
Cost of sales (GAAP) FY2026 ≈$1.7B, including $0.9B non-recurring litigation settlement charge ≈$1.8B Lowered
Research and development expense (GAAP) FY2026 ≈$2.9B ≈$3.0B Lowered
Selling, general and administrative expense (GAAP) FY2026 ≈$1.0B — —
Income tax expense FY2026 Negligible — —
Capital expenditures FY2026 $0.2B-$0.3B — —
Cash and investments Year-end 2026 $4.7B-$5.2B — Improved by ≈$0.2B

Investor Takeaways

  • Watch the August 5, 2026 PDUFA date for mFLUSIVA and whether it receives U.S. approval.
  • Moderna expects potential 2026 data from its Phase 3 adjuvant melanoma study and its propionic acidemia registrational study.
  • The ongoing norovirus Phase 3 trial will enroll an additional cohort after missing statistical criteria for early success at interim analysis.

The summary is written by an AI model reading the filing.

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