A Phase 3 Open-Label, Single-Arm Study to Evaluate the Safety and Immunogenicity of an Omicron JN.1 Subvariant SARS-CoV-2 rS Vaccine Adjuvanted With Matrix-M

A Phase 3 Open-Label, Single-Arm Study to Evaluate the Safety and Immunogenicity of an Omicron JN.1 Subvariant SARS-CoV-2 rS Vaccine Adjuvanted With Matrix-M

Publication date: Jul 14, 2025

This study is a Phase 3 trial designed to check the safety and immune response to a new Omicron JN. 1 COVID-19 vaccine. Study researchers will give a single dose of this vaccine, called NVX-CoV2705, to approximately 120 participants. This includes adults aged 65 and older, and individuals aged 12 to 64 who have existing health conditions that put them at high risk for severe COVID-19. All participants must have received a previous COVID-19 vaccine at least 90 days before joining this study. Study researchers will be closely monitoring participants for their immune response for 28 days and collecting safety data for 180 days after vaccination.

Concepts Keywords
Coronavirus COVID-19
Myocarditis
Nanoparticle
Vaccinated

Semantics

Type Source Name
disease IDO immune response
disease MESH COVID-19
disease MESH amenorrhea
disease IDO country
drug DRUGBANK Levonorgestrel
disease MESH lifestyle
disease MESH health status
disease IDO history
disease MESH hypertension
disease MESH allergies
disease MESH anaphylaxis
disease MESH myocarditis
disease MESH pericarditis
disease MESH alcohol abuse
disease MESH drug addiction
disease IDO immunodeficiency
disease MESH thyroiditis
disease MESH pancreatitis
disease MESH stable diabetes mellitus
disease MESH diabetic ketoacidosis
drug DRUGBANK Prednisone
drug DRUGBANK Tacrolimus
drug DRUGBANK Ciclosporin
disease IDO blood
disease MESH cancer
disease MESH carcinoma
disease MESH lentigo maligna
drug DRUGBANK Methylergometrine
disease MESH carcinoma in situ
disease IDO quality
disease IDO site
disease MESH sore throat
pathway REACTOME SARS-CoV-2 Infection

Original Article

(Visited 7 times, 1 visits today)