
The US company said it expected to release preprint data in the coming week, with live virus data to follow.
Based on pseudovirus and extensive pharmacokinetic data, the company said it believed the 500mg dose of sotrovimab is sufficient to retain activity against the BA.2 variant, which is in line with all other variants of concern and interest.
The monoclonal antibody therapy, sotrovimab, is authorised for emergency use in the US.
The companies are sharing the latest data with global regulatory authorities, Vir said.
Sotrovimab is one of the few Covid-19 treatments shown to have worked against the fast-spreading Omicron variant, spurring demand.
It was amongst GSK’s top-selling offerings last year.