CAMBRIDGE (CBS) — Days after Pfizer received FDA backing for its COVID vaccine, Moderna has submitted an application for full approval of its own two-dose shot regimen.
The Cambridge-based biotech company says a final study of its mRNA vaccine shows it is 93% effective against the coronavirus for six months after a second dose.READ MORE: Topsfield Fair Returns Friday After Year Off Due To Pandemic
“This BLA submission for our COVID-19 vaccine, which we began in June, is an important milestone in our battle against COVID-19 and for Moderna, as this is the first BLA submission in our company’s history,” CEO Stéphane Bancel said in a statement.READ MORE: MBTA Says Inspectors Checked Escalator 3 Weeks Before It Malfunctioned
The Moderna vaccine is currently available to anyone 18 years and older under Emergency Use Authorization. Moderna is seeking emergency use authorization for the vaccine on adolescents 12 and older. Nearly 65 million in the United States have been fully vaccinated via Moderna, according to the CDC.
Pfizer finished its application to the FDA in May; approval for Moderna could take months.MORE NEWS: I-Team: Consumers Report Car Dealers For Using Deceptive Advertising Tactics
A recent CDC study found that COVID vaccines are less effective against the highly contagious Delta variant, but still reduce infection risk by about two-thirds.