By Pushkala Aripaka
(Reuters) -Britain's health regulator on Wednesday approved the country's first two-pronged COVID-19 booster targeting the Omicron BA.4 and BA.5 sub-variants and the original coronavirus strain.
The Medicines and Healthcare products Regulatory Agency (MHRA) said the vaccine from Pfizer (NYSE:PFE) and partner BioNTech was approved for use as a booster in people 12 years and older after it was found to meet safety, quality and effectiveness standards.
Britain had already approved so-called bivalent vaccines targeting the Omicron BA.1 sub-variant from Pfizer-BioNTech and rival Moderna (NASDAQ:MRNA), but now has added a first against BA.4/5 in its arsenal with the latest authorisation.
The regulator on Wednesday also approved Novavax (NASDAQ:NVAX)'s COVID-19 shot as a booster for adults.
"All approved COVID booster vaccines help to improve the protection obtained from earlier doses of the vaccine and help give longer-term protection against getting seriously ill from COVID-19," the MHRA said.
The UK has recorded more than 23 million COVID-19 infections and over 190,000 deaths, the seventh-highest globally, according to the World Health Organization (WHO), with about 150 million vaccine doses having been given by early September for a population of around 67 million.
Omicron sub-variants BA.4/5 dominated the summer and are still behind the majority of infections globally, but newer Omicron sub-variants are gaining ground, with hundreds of them being tracked by scientists, WHO officials said last month.
While existing COVID-19 vaccines continue to provide good protection against hospitalisation and death, vaccine effectiveness has taken a hit as the coronavirus, which originally emerged in China in December 2019, has evolved.
Warnings over a possible "twindemic" of COVID-19 and flu have also been issued by UK officials after the end of restrictions meant increased social contact.
Pfizer and BioNTech last week said their shot tailored to BA.4/5 produced a strong antibody response in older adults than the original shot after one month, and in October said it generated a strong immune response.
Healthcare regulators for the European Union, the United States and Canada had already approved the retooled Pfizer-BioNTech shot last month.