Moderna, Inc.

Moderna, Inc. Earnings Recaps

MRNA Health Care 2 recaps
Q1 2026 May 4, 2026

Moderna’s shares rose 3.0% following a quarter marked by solid international revenue growth and significant cost reductions, offsetting the expected impact from a large litigation settlement charge.

Key takeaways
  • Reported Q1 revenue of $400 million, driven primarily by international markets (80%), notably from long-term strategic partnerships with the U.K. government.
  • Company reiterated full-year revenue growth guidance of up to 10% for 2026, supported by strong early performance and new product approvals in the EU.
  • Recognized a substantial $878 million litigation settlement charge in cost of sales during the quarter, resulting in a GAAP net loss of $1.3 billion; excluding this item, net loss declined by over 50% year-over-year.
  • Adjusted cash costs fell 26% year-over-year to align with the target of approximately $4.2 billion for the full year, reflecting sustained cost discipline across R&D and SG&A.
  • Pipeline progress includes EU approvals for two new vaccines, initiation of a Phase III trial in early-stage lung cancer, and ongoing Phase II/III studies in oncology and pandemic flu vaccines.
Q3 2025 Nov 6, 2025

Moderna reported third-quarter 2025 revenues of $1 billion, highlighting a significant ongoing focus on cost reductions despite a net loss of $200 million, driven by lower COVID vaccine demand.

Key takeaways
  • Revenue declined 45% year-over-year, reflecting decreased demand for COVID vaccines; U.S. revenues were particularly impacted.
  • Cost of sales, R&D, and SG&A combined saw a 34% reduction compared to Q3 2024, yielding a $2.1 billion improvement over the last four quarters.
  • Phased approvals for the mNEXSPIKE and mRESVIA vaccines were expanded, cementing partnerships and local manufacturing capabilities in key markets.
  • Full-year 2025 revenue guidance narrowed to $1.6 billion–$2 billion; fourth-quarter U.S. revenue projected at $100 million–$400 million.
  • CMV vaccine development was discontinued after failing to meet primary efficacy endpoints, impacting future pipeline dynamics.