Reuters news agency reported on Wednesday that the US government will buy 1.25 million additional doses of Regeneron Pharmaceuticals' COVID-19 antibody cocktail for about USD2.63bn. thereby bringing the total supply of the treatment to over 1.5 million doses.
Reportedly, this cocktail, a combination of two antibodies casirivimab and imdevimab, was authorised in November 2020 for emergency use by the US Food and Drug Administration.
The US Department of Health and Human Services (HHS) said the doses will be delivered in the first half of 2021 to treat non-hospitalised, high-risk COVID-19 patients.
In a statement, HHS Assistant Secretary for Preparedness and Response, Robert Kadlec, said: "With COVID-19 cases continuing to rise, treating people with mild or moderate infections can help prevent hospitalisations."
The Regeneron treatment is part of a class of drugs known as monoclonal antibodies, which are manufactured copies of antibodies created by the human body to fight infections.
Earlier this week, Regeneron had said its therapy will likely be effective against new variants of the COVID-19 virus identified so far in a handful of countries.
Also, Eli Lilly's antibody treatment has also been authorised for emergency use by the regulator, Reuters added.
The HHS Office of the Assistant Secretary for Preparedness and Response (ASPR) said on 12 January 2021 that to date, it has allocated over 127,700 treatment courses of the therapy.
BRC Therapeutics participates in regulators' workshop advancing botanical drug development
Lupin announces receipt of US FDA tentative approval for Apixaban Oral Suspension
QIAGEN completes US QIAstat-Dx bloodstream infection portfolio with FDA clearance
Innovent expands global Phase 3 study of IBI363/TAK-928 to include non-squamous NSCLC
FDA approves WELIREG and LENVIMA combination for previously treated advanced renal cell carcinoma
AstraZeneca's IMFINZI combination receives US Priority Review for muscle-invasive bladder cancer
XtalPi submits US FDA IND application for KQTD-126 in chronic intestinal pain
Revvity launches IVDR-certified solution for early detection of type 1 diabetes
FDA Advisory Committee votes in favour of GRAIL's Galleri multi-cancer early detection test
AstraZeneca's Trixeo Aerosphere approved in EU for asthma maintenance treatment