Stock Markets February 26, 2026

Novavax Lifts 2026 Adjusted Revenue Outlook as Licensing and Supply Milestones Offset Weak Demand

Company posts fourth-quarter profit and points to Sanofi collaboration and adjuvant licensing as drivers of future growth

By Derek Hwang NVAX MRNA SNY PFE
Novavax Lifts 2026 Adjusted Revenue Outlook as Licensing and Supply Milestones Offset Weak Demand
NVAX MRNA SNY PFE

Novavax raised its adjusted revenue guidance for 2026 after securing expectations for milestone payments tied to vaccine supply and licensing arrangements, even as demand for COVID-19 shots remains muted. The biotech reported a swing to profit in the fourth quarter, supported by cost reductions and licensing deals that helped soften the impact of U.S. policy changes on vaccination rates.

Key Points

  • Novavax raised its 2026 adjusted revenue guidance to $230 million - $270 million, up from $185 million - $205 million; this excludes sales and royalties from its Sanofi partnership.
  • The company recorded a fourth-quarter profit with revenue up 67% to $147 million and net income of $18 million versus a $81 million loss a year earlier.
  • Licensing deals, including a Matrix-M adjuvant license to Pfizer worth up to $530 million and product launches with Sanofi, underpin the company’s plan to reach profitability by 2028.

Novavax said on Thursday that it is increasing its adjusted revenue projection for 2026, citing anticipated milestone payments from vaccine supply and licensing agreements that management expects will counterbalance the effects of weaker demand for COVID-19 vaccines.

The company now forecasts 2026 adjusted revenue in a range of $230 million to $270 million, up from its earlier outlook of $185 million to $205 million. Novavax noted that those figures do not include sales and royalties from its collaboration with Sanofi.

Management linked part of the demand pressure to a pronounced change in U.S. vaccine policy, noting that the shift has reduced vaccination rates and altered the regulatory environment for new shots. On that point, Novavax’s CEO said, "We probably disagree as a scientific community and an industry with some of their positions," adding that they "do see a pathway forward".

Recent regulatory developments involving a rival also drew comment from Novavax leadership. The company referred to an episode in which the U.S. Food and Drug Administration initially declined to review Moderna’s mRNA-based flu vaccine and then reversed that decision a week later after Moderna amended its application. "It was good to see them (Moderna) have a regulatory path forward for their flu vaccine," the CEO said.

Novavax flagged several contributors to its updated outlook and longer-term plans. The company expects to reach profitability by 2028 and cited planned product launches tied to its Sanofi agreement, including a COVID-flu combination vaccine that incorporates Novavax’s Nuvaxovid shot. In addition, Novavax last month licensed its Matrix-M adjuvant to Pfizer in a deal worth up to $530 million; the adjuvant is designed to enhance immune response to vaccine antigens.

Management also reported heightened commercial interest in the company’s platform, observing, "We have more interest than I’ve ever seen in three years in our tech and some great conversations going on."

On the results front, Novavax said fourth-quarter revenue rose 67% to $147 million, exceeding the analysts' average estimate of $78.84 million compiled by LSEG. The company posted net income of $18 million for the quarter, reversing a net loss of $81 million in the year-earlier period.


Outlook and considerations

Novavax’s upward revision to 2026 adjusted revenue reflects a recalibration toward milestone-driven cash inflows and licensing proceeds rather than near-term broad-based sales growth for COVID-19 shots. While the company is projecting a path to profitability by 2028 anchored on collaboration-driven product launches and adjuvant monetization, regulatory shifts and vaccination trends remain key variables to monitor.

Risks

  • Restrictive U.S. vaccine recommendations and consequent falling vaccination rates could continue to depress demand for COVID-19 shots - impacts vaccine manufacturers and public health sectors.
  • Regulatory uncertainty, illustrated by the FDA's initial refusal and subsequent reversal on a rival's flu vaccine application, introduces timing and approval risk for new vaccine candidates - affects biotech firms seeking approvals.
  • Reliance on milestone payments and licensing income makes revenue contingent on successful execution of partner agreements and product launches - impacts company financial stability and investor expectations.

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