Drug intelligence / Profile preview

respiratory syncytial virus vaccine (recombinant, adjuvanted)

Development stage
Approved
Lead developer
GSK
Modality
Recombinant Proteins and Enzymes, Vaccines & Immunotherapeutics
Administration
Intramuscular
01

Overview

Arexvy is a recombinant subunit vaccine developed by GSK to prevent lower respiratory tract disease (LRTD) caused by respiratory syncytial virus (RSV) in adults aged 60 years and older. It consists of a stabilized pre-fusion conformation of the RSV F protein (RSVPreF3) combined with GSK's proprietary AS01E adjuvant system. The AS01E adjuvant, which contains 3-O-desacyl-4'-monophosphoryl lipid A (MPL) and QS-21 in a liposomal formulation, is designed to enhance the T-cell and antibody response to the antigen. By targeting the pre-fusion state of the F protein—the primary target for neutralizing antibodies—the vaccine elicits a robust immune response against both RSV-A and RSV-B subtypes. It was the first RSV vaccine to receive regulatory approval globally.

Brand names
Arexvy
Other names
RSVPreF3 + AS01ERSVPreF3RSVPreF-3RSVPreF 3RSVPreF3 OARSVPreF-3 OARSVPreF 3 OARecombinant Respiratory Syncytial Virus Pre-fusion F Protein Vaccine
02

Targets

RSV F (Respiratory syncytial virus fusion protein)

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