RSV (Respiratory Syncytial Virus) Vaccination
Arexvy (manufactured by GSK) is the first ‘respiratory syncytial virus’ (RSV) vaccine for adults authorised in the UK, EU and USA.
CDC recommends RSV vaccine for older adults.
Trial findings
Safety
- The local administration site adverse reactions reported with Arexvy had a duration of 2 days on average.
- The systemic adverse reactions (fatigue, muscle aches and pain, headache, joint pain and fever) reported with Arexvy had duration ranging between 1 and 2 days.
- Similar rates of serious adverse events (4.2% vs 4.0%), deaths (0.4% vs 0.5%), and F (0.3% vs 0.3%) were reported between participants who received Arexvy (n=12,467) and placebo (n=12,499), respectively.
RSV is a common respiratory virus that usually causes mild cold-like symptoms but can be serious in vulnerable people including babies, older adults, and those with underlying conditions such as diabetes.
This vaccine authorisation from the medicines regulators is based on data from a randomised, placebo controlled trial in 25 000 adults aged over 60 in 17 countries.
The study is ongoing and will be used to evaluate the efficacy of a single vaccine dose over multiple seasons, the need for re-vaccination, and the vaccine’s safety profile. GSK is also carrying out a clinical trial that aims to expand the population who may benefit from RSV vaccine to adults aged 50-59, including those with underlying comorbidities, and results are expected this year.
(from an article in the BMJ: https://www.bmj.com/content/381/bmj.p978)
See the official insert of this vaccine here.
GSK press release: https://tinyurl.com/39j479dh