FDA authorizes COVID-19 antigen test with 15-minute turnaround time

Katie Adams - Print  | 

The FDA on Aug. 26 granted emergency use authorization to Abbott's COVID-19 antigen test that presents results on a testing card in just 15 minutes, operating similarly to a pregnancy test.

The test is authorized for point-of-care settings, such as physician offices, emergency rooms and certain schools. Healthcare providers using Abbott's test will swab a patient's nose, transfer the sample to a test card and wait 15 minutes to read the results directly from the card.

"This means people will know if they have the virus in almost real-time. Due to its simpler design and the large number of tests the company anticipates making in the coming months, this new antigen test is an important advancement in our fight against the pandemic," Jeff Shuren, MD, director of the FDA's Center for Devices and Radiological Health, said in a news release.

Abbott said it plans to make up to 50 million tests per month available in the U.S., beginning in October.

The FDA news release noted that antigen tests, while generally specific, are not as sensitive as molecular ones, and their results should be taken into consideration along with relevant clinical observations, patient history and epidemiological knowledge.

More articles on pharmacy:
US sues Teva for 2nd time in 1 week, this time for alleged price-fixing scheme
FDA delays collecting drugmaker data required by CARES Act
Acadia Pharmaceuticals acquires Texas drugmaker for $52.5M, expands non-opioid painkiller portfolio


© Copyright ASC COMMUNICATIONS 2021. Interested in LINKING to or REPRINTING this content? View our policies by clicking here.