CDC Director Rochelle P. Walensky, MD, MPH, signed a decision memo saying the vaccine can be used as third option for primary COVID-19 vaccination in this age group. The FDA issued an emergency use authorization (EUA) for the vaccine on Friday.
The two-dose, protein-based vaccine differs from the Pfizer-BioNTech and Moderna messenger RNA vaccines, which are available for children as young as age 6 months.
Experts have said that the availability of a non-mRNA vaccine could help reduce COVID-19 vaccine hesitancy.
According to phase 3 trial results Novavax released in February, overall vaccine efficacy in a cohort of more than 2,200 adolescents was 79.5% against PCR-positive mild, moderate or severe COVID-19 cases occurring 7 days or more after the second dose. Efficacy was consistent between two age groups — 12 to 14 years and 15 to 17 years.
Stanley C. Erck, president and CEO of Novavax, said the EUA would “hopefully help increase vaccination rates, particularly as we prepare for ongoing surges of COVID-19 with the start of fall and the back-to-school season.”
“We hope that our vaccine, developed using an innovative approach to recombinant protein vaccine technology, may have a special role in adolescent vaccination based on parents' and caregivers' familiarity with protein-based vaccines used in other disease areas,” Erck said.
The FDA granted an EUA for the vaccine in adults last month.