Moderna lifts full-year sales outlook as flu shot approval and 29% quarterly growth offset $950m settlement
The mRNA specialist now expects 2026 revenue to grow 15–25%, against a prior ceiling of 10%, while a norovirus setback and a litigation payment temper the update.
Moderna has materially raised its revenue outlook for 2026. Alongside third-quarter results on 6 November, the company said it now expects full-year sales growth of 15% to 25%. Its earlier guidance pointed to growth of no more than 10%.
The quarter itself brought revenue of $1.3 billion and net income of $162 million, with sales up 29%. The material available does not say what drove that increase or what period it is measured against, so the split between products and markets is unclear.
The commercial backdrop includes the US Food and Drug Administration's August approval of mFLUSIVA, Moderna's mRNA influenza vaccine. Approval is full for adults aged 50 to 64 and accelerated for those 65 and older. Moderna also reported Canadian approval of mCOFLU. No pricing, launch timing or sales expectations for either product were included in the information available.
In oncology, Moderna cited positive Phase 3 melanoma results for intismeran, which is given with Merck's Keytruda. Details of the data were not provided. Less welcome was an interim analysis of its norovirus vaccine candidate, which fell short of the test for declaring early success.
Moderna also noted a $950 million payment to settle litigation. The terms of the settlement and its treatment in the quarter's accounts were not available. Context: accelerated approvals generally come with obligations to confirm benefit in follow-up studies, a point relevant to the 65-plus label.
Why it matters
- The guidance change, from growth of up to 10% to 15–25%, is a large shift in Moderna's own expectations for 2026, though the drivers were not disclosed.
- mFLUSIVA's split label, full for 50–64 and accelerated for 65+, means payers and market-access teams may weigh different evidence by age group.
- The norovirus interim miss leaves that programme's timeline uncertain, while the melanoma result adds to the oncology case for intismeran with Keytruda.
- The $950 million settlement is a significant cash item, but without terms or accounting detail its effect on the financial picture cannot be judged.
Company's press release (SEC filing): Moderna, Inc. ↗
Written by CompePharma's editorial system from the company's filing; claims are the company's. AI-assisted; check the source before acting. Not investment advice.