Johnson & Johnson announced that the U.S. Centers for Disease Control and Prevention (CDC) Advisory Committee on Immunization Practices (ACIP), has recommended its COVID-19 vaccine as a booster for all eligible individuals who receive an authorized COVID-19 vaccine.

"Today's recommendation supports the use of the Johnson & Johnson COVID-19 vaccine as a booster for eligible individuals in the U.S. regardless of which vaccine they initially receive," said Paul Stoffels, M.D., Vice Chairman of the Executive Committee and Chief Scientific Officer at Johnson & Johnson. "The Johnson & Johnson vaccine provided 94 percent protection in the U.S. against COVID-19 when given as a booster following the single-shot Johnson & Johnson vaccine, and due to its unique mechanism of action, offers long-lasting, durable protection. We remain confident in the benefit it will provide to millions around the world."

The Johnson & Johnson COVID-19 vaccine was recommended as a booster for adults aged 18 and older who received the Johnson & Johnson single-shot vaccine at least two months earlier. A booster dose of the Johnson & Johnson COVID-19 vaccine was also recommended for eligible adults at least six months following the second dose of an authorized mRNA vaccine.

The ACIP recommendation has been forwarded to the Director of the CDC and the U.S. Department of Health and Human Services (HHS) for review and adoption.

The Company's single-dose COVID-19 vaccine received FDA Emergency Use Authorization  for adults aged 18 and older on February 27, 2021. On October 20, 2021, the FDA authorized for emergency use a booster shot of the Johnson & Johnson COVID-19 vaccine for adults aged 18 and older at least two months following primary vaccination with the Company's single-dose vaccine.