Piscataway-based GenScript USA Inc. said Monday that the U.S. Food and Drug Administration (FDA) granted Emergency Use Authorization (EUA) for the cPass™ SARS-CoV-2 Neutralization Antibody Detection ...

Antibody tests weren't meant to gauge COVID-19 vaccine immunity. Dr. Anthony Fauci said they also wouldn't be the best sign you need a booster.

SAN FRANCISCO -- There has been a lot of talk about testing for the coronavirus, but you may not entirely understand what the different tests are for. The coronavirus makes some people sick, some ...

Although the 'emergency' phase of the COVID-19 pandemic may be over, it is still ongoing, and thousands of people still die from the disease every week. The virus also continues to mutate, and new ...

(Reuters) - LabCorp said on Thursday it has launched a new test that could assess the capacity of antibodies in patient plasma to inhibit the novel coronavirus. Information from the test about the ...

The FDA has issued emergency authorizations to 12 antibody tests for the virus. As federal officials gradually begin reopening the country, expanded testing is central to the conversation. Until now, ...

BOSTON & TORONTO--(BUSINESS WIRE)--Virna Therapeutics announces that they are partnering with University of Toronto to in-license neutralizing antibodies, to treat COVID-19. The discovery was made in ...

"We feel this pressure because we want to help people." Antibody tests, which reveal whether someone has been infected with the novel coronavirus, have been touted as key to reopening the economy and ...

The FDA issued an emergency use authorization (EUA) for pemivibart (Pemgarda) as COVID-19 pre-exposure prophylaxis in immunocompromised individuals who are unlikely to mount a sufficient immune ...

In a recent study published in the journal Annals of Internal Medicine, researchers investigated whether short-term adverse effects of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ...