Moderna says it plans to seek emergency use authorization from the U.S. Food and Drug Administration for its COVID-19 vaccine in children under age 6.

Moderna is seeking emergency use authorization from the US Food and Drug Administration for its Covid-19 vaccine for children 6 months through 5 years of age, the company said Thursday.

Biotech company Moderna applied Monday for an emergency use authorization from the U.S. Food and Drug Administration after receiving more good news about the safety and effectiveness of its ...

Drugmaker Moderna says it has applied to the Food and Drug Administration for emergency use authorization for its coronavirus vaccine. It says data bolster its case the vaccine is safe and effective.

Once emergency use authorization is granted, Moderna will begin shipping millions of doses, earmarked for health workers and nursing home residents, to boost the largest vaccination effort in U.S ...

Moderna on Thursday requested emergency use authorization from the Food and Drug Administration for a fourth dose of its COVID-19 vaccine as a booster for people 18 and over — a broader request ...

the US now has a second vaccine. The FDA Friday evening, authorizing emergency use for Moderna Peter Jackson of Marble, had already got the vaccine taking part in the Moderna trials. Covic ...

Moderna announced Monday it will ask the Food and Drug Administration for emergency use authorization (EUA) for its COVID-19 vaccine, making it the second company, after Pfizer, to seek EUA for a ...

Moderna Files for Emergency Use Authorization for its COVID-19 Vaccine in Adolescents in the United States. Submission based on Phase 2/3 study of mRNA-1273 in adolescents ages 12 to less than 18 ...

CAMBRIDGE (CBS) -- Moderna on Thursday announced it has filed for emergency use authorization of its COVID vaccine in adolescents 12 to 17 years old. This comes after a study showed its vaccine ...

PHILADELPHIA (CBS) -- A COVID-19 vaccine for young children could be on the way. Moderna on Thursday submitted a request to the U.S. Food and Drug Administration for emergency use authorization ...