WASHINGTON (REUTERS) - The United States has signed contracts worth roughly US$1 billion (S$1.35 billion) to secure the antibody-based Covid-19 treatment sotrovimab from GSK and Vir Biotechnology , the drugmakers said on Wednesday (Nov 17), with supply expected by Dec 17.
Britain's GSK said the deal brought the total number of doses secured of the treatment, branded Xevudy, to more than 750,000 globally, adding that the United States would have an option to buy additional doses through March 2022.
The companies did not specify how many doses the US government had signed up for. However, other deals include 10,000 doses for Canada and up to 220,000 doses for the European Union.
Sotrovimab is authorised for emergency use in the United States to prevent mild or moderate cases of Covid-19 from worsening. The European Medicines Agency has given its go-ahead for use by member states although EU-wide approval is still pending.
The treatment has shown to cut the risk of hospitalisation or death by 79 per cent in adults with mild-to-moderate Covid-19.
While vaccines remain at the heart of the fight against Covid-19, treatments including oral antiviral pills offer options to contain infections.
Last week, partners GSK and Vir said the drug was shown in a trial to work as well when given as a shot in the arm when administered via the standard infusion, potentially offering more convenience.
"Given ongoing evidence, which demonstrates its ability to maintain activity against the tested circulating variants of concern, including Delta, we are confident sotrovimab will continue to be important," Vir's Chief Executive George Scangos said in a statement.
The US Food and Drug Administration in May gave an emergency use authorisation to the GSK-Vir treatment for treating mild-to-moderate Covid-19 in people aged 12 years and older, who are at the risk of their illness worsening.
The treatment, branded Xevudy, had brought in sales of £130 million (S$237 million) for GSK in the first nine months of 2021.
Similar products are offered or being developed by Eli Lilly, Regeneron and AstraZeneca.
