Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
NVX-CoV2373 + Matrix-M is a **combination COVID-19 vaccine** composed of a recombinant, prefusion-stabilized, full-length SARS-CoV-2 spike protein nanoparticle (NVX-CoV2373) formulated with the Matrix-M adjuvant. The vaccine leverages a **baculovirus/Sf9 insect cell expression system** to produce spike protein nanoparticles that closely mimic the native viral antigenic structure. Matrix-M is a saponin-based adjuvant made from *Quillaja saponaria* fractions (Matrix-A and Matrix-C nanoparticles), engineered to stimulate robust Th1-skewed cell-mediated and humoral immune responses by enhancing antigen presentation and immune cell activation at the injection site and draining lymph nodes. NVX-CoV2373 + Matrix-M induces high titers of neutralizing antibodies, CD4+ and CD8+ T cells, and memory B cells, providing protection against SARS-CoV-2 infection. It is approved or authorized in multiple countries for the prevention of COVID-19 in adults and has demonstrated efficacy and safety in phase III clinical trials[1][2][3][4][5][6].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on NVX-CoV2373 + Matrix-M.