(Reuters) – The European Medicines Agency (EMA) will hold an extraordinary meeting on Sept. 1 to discuss applications from Moderna and Pfizer for vaccine boosters modified to target the Omicron variant, the regulator said on Tuesday.
The new so-called bivalent shots combat the BA.1-subvariant of Omicron and the original virus first detected in China.
Britain earlier this month became the first country to clear Moderna’s shot, which is also the world’s first bivalent vaccine.
(Reporting by Radhika Anilkumar in Bengaluru; Editing by Devika Syamnath)