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01

Nuvaxovid™ 2025-2026 Formula COVID-19 Vaccine Approved in the U.S.

Nuvaxovid™ is the only protein-based, non-mRNA COVID-19 vaccine available in the U.S. for the 2025-2026 vaccination season

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02

Q2 Financial Results and Operational Highlights

Novavax reported progress on its growth strategy and three strategic priorities.

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03

Novavax Reports CIC and Stand-alone Influenza Phase 3 Trial Results

Novavax’s COVID-19-Influenza Combination and Stand-alone Influenza Vaccine Candidates Showed Robust Immune Responses and Were Well Tolerated in Initial Cohort of a Phase 3 Trial

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A Proven Platform

Our proprietary cutting-edge technology platform is revolutionizing the development of vaccines to help prevent some of the world's most challenging diseases.

Combining Novavax’s protein-based nanoparticles with our Matrix-M® adjuvant achieves strong, long-lasting and broad immune responses.1

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Protein-based Nanoparticles

Our protein-based nanoparticles are made of engineered proteins of the target pathogen used to trigger immune system recognition.2

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Matrix-M® Adjuvant

Our Matrix-M adjuvant enhances the body's immune response in a targeted and efficient way, significantly improving both the magnitude and the duration of immune response.1

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Our Pipeline

We are advancing a pipeline of high-value assets targeting areas with unmet medical needs, strong scientific rationale and significant commercial potential.

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High-Impact Partnerships

Our strategy is to create partnership and collaboration opportunities to maximize the impact and value of our pipeline assets and Matrix-M alone.

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Latest News

Keep up to date on the latest happenings at Novavax as we tackle the world’s most significant health needs.

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Investors

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  1. Stertman L. et al.; The Matrix-M™ adjuvant: A critical component of vaccines for the 21st century. Hum Vaccin Immunother. 2023 Dec 31;19(1):2189885. doi: 10.1080/21645515.2023.2189885.
  2. Nguyen B. Tolia N; Protein-based antigen presentation platforms for nanoparticle vaccines. NPJ Vaccines. 2021 May 13;6(1):70. doi: 10.1038/s41541-021-00330-7