Key highlights:
- Authorisation will help protect adults 60 years of age and older in the UK from RSV disease for the first time.
- In the UK, RSV leads to an estimated 14,000 hospitalisations and an estimated 8,000 deaths in adults 60 years of age and older each year.
- The authorisation is based on phase III efficacy data in older adults.
GSK announces that the Medicines and Healthcare products Regulatory Agency (MHRA) has authorised Arexvy (respiratory syncytial virus vaccine, adjuvanted) for active immunisation for the prevention of lower respiratory tract disease (LRTD) caused by respiratory syncytial virus (RSV) in adults 60 years of age and older. This is the first time an RSV vaccine for older adults has been authorised for use in Great Britain by the MHRA.
Neale Belson, Senior Vice President, and General Manager UK at GSK said: “We are very excited by the announcement. Our ambition is to help protect adults 60 years of age and older in the UK who are at risk from RSV disease, including those with underlying medical conditions, who drive the majority of RSV hospitalisations. This authorisation for Arexvy means eligible adults can be vaccinated against RSV disease for the first time, reinforcing GSK’s long history of vaccine innovation.”
RSV is a common, contagious respiratory virus that leads to an estimated 175,000 GP visits, 14,000 hospitalisations, and 8,000 deaths each year in adults aged 60 years and over in the UK. Recent studies indicate that the burden of RSV disease may be even greater than that of influenza in hospitalised older adults. Those with underlying medical conditions, such as diabetes and chronic heart and lung disease, drive the majority of RSV hospitalisations.
The authorisation is supported by data from the pivotal AReSVi-006 (Adult Respiratory Syncytial Virus) phase III vaccine efficacy trial, published in the New England Journal of Medicine. In this trial, there was high overall vaccine efficacy against RSV-LRTD, including in participants with certain underlying medical conditions.
The vaccine was generally well tolerated. The most frequently observed solicited adverse events were injection site pain, fatigue, myalgia, arthralgia, and headache. These were generally mild to moderate and transient. The MHRA’s decision follows the European Commission’s authorisation of Arexvy on 6 June 2023. GSK’s marketing authorisation application in the EU was reviewed under the accelerated assessment mechanism because prevention of RSV illness in the older adult population is considered a major public health interest.
Arexvy was the world’s first RSV vaccine for older adults to be approved by the US Food and Drug Administration. Regulatory reviews are ongoing in Japan and several other countries.
About Arexvy (Respiratory Syncytial Virus (RSV) vaccine (recombinant, adjuvanted))
Respiratory syncytial virus vaccine, adjuvanted, contains recombinant glycoprotein F stabilised in the prefusion conformation (RSVPreF3). This antigen is combined with GSK’s proprietary AS01 adjuvant.
Indication
The MHRA has authorised Arexvy for active immunisation for the prevention of LRTD caused by RSV in adults aged 60 years and older. It is also approved in the US and in member states of the European Union and the European Economic Area (EEA). The use of this vaccine should be in accordance with official recommendations. As with any vaccine, a protective immune response may not be elicited in all vaccinees.
The proposed trade name remains subject to regulatory approval in other markets.
A clinical trial investigating RSV vaccination in adults aged 50-59, including participants with underlying comorbidities, is fully recruited. Results are expected in 2023, together with additional results from the AReSVi-006 phase III efficacy trial and the AReSVi-004 immunogenicity trial. These trials continue to evaluate an annual revaccination schedule and protection/immunogenicity over multiple seasons following one dose of the RSV vaccine.
The GSK proprietary AS01 adjuvant system contains QS-21 STIMULON adjuvant licensed from Antigenics Inc, a wholly owned subsidiary of Agenus Inc.
About AReSVi-006
This is a randomised, placebo-controlled, observer-blind, multi-country phase III trial to demonstrate the efficacy of a single dose of GSK's adjuvanted RSVPreF3 vaccine in adults aged 60 years and above. Approximately 25,000 participants were enrolled from 17 countries. Initial results were published in the New England Journal of Medicine in February 2023.