Yorkshire firm Avacta's rapid fire highly accurate lateral flow test approved for UK use by regulators
US firm Avacta's rapid fire highly accurate lateral flow test approved for UK use by regulators
US firm Avacta has received approval from Britain’s Medicines and Healthcare products Regulatory Agency (MHRA) to bring its rapid fire Covid testing product to market.
The Wetherby firm’s Avacta’s AffiDX® SARS-CoV-2 antigen lateral flow test is said by Avacta to be significantly more accurate than other quick delivery testing for the virus.
The product registration by the MHRA allows the Company to sell the product in the UK for professional use and the Company expects product registration from a Competent Authority within the EU to follow shortly.
ike other lateral flow antigen tests, Avacta’s product is intended to provide a cost effective and rapid means of identifying individuals with a high viral load that means they are more likely to infect others.
The clinical data for Avacta’s AffiDX® SARS-CoV-2 antigen lateral flow test reported in April demonstrated 100 per cent sensitivity for identifying infectious individuals with viral loads measured by PCR of Ct<27.
Avacta said it was now involved in multiple ongoing commercial discussions with distributors and end user customers in countries that accept the CE mark for in vitro diagnostic products.
Dr Alastair Smith, Chief Executive Officer of Avacta Group, said: “I am delighted to receive confirmation of the registration of the AffiDX SARS-CoV-2 antigen test from the MHRA. It is a transformative milestone for Avacta’s Diagnostics Division being the first CE marked product powered by the Affimer platform that has been brought to market.
“The excellent results of the recent clinical evaluation of the test at a clinical site in Europe demonstrate the test has excellent sensitivity across a range of viral loads, which would be considered infectious.
” As part of the study the same clinical samples were tested with two leading, commercially available lateral flow antigen tests, and the data show that the AffiDx® test has superior clinical sensitivity across the range of samples and in particular at lower viral loads.
“We are very excited by the potential of this high-quality SARS-CoV-2 rapid antigen test and by the interest it has already attracted from potential commercial partners and distributors . We will continue to focus on its commercial roll-out and manufacturing scale-up to meet demand.
“Lateral flow tests have a crucial role to play in helping our society and economy return to normal, and I am confident that the AffiDX® test will now play a significant part in this process.”
