US launches study mixing COVID-19 booster vaccine regimens

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The National Institutes of Health (NIH) has initiated an early-stage study testing mixed COVID-19 booster vaccine schedules among fully vaccinated adults. The goal is to understand safety and immune responses following mixed boosted regimens, should booster vaccines become necessary.

The NIAID-funded study involves some 150 people who already received one of the authorized COVID-19 vaccine regimens developed by Pfizer, Moderna or Johnson & Johnson.

“Although the vaccines currently authorized by the U.S. Food and Drug Administration offer strong protection against COVID-19, we need to prepare for the possibility of needing booster shots to counter waning immunity and to keep pace with an evolving virus,” Dr. Anthony S. Fauci, director of the National Institute of Allergy and Infectious Diseases (NIAID), said in a release posted Tuesday. “The results of this trial are intended to inform public health policy decisions on the potential use of mixed vaccine schedules should booster doses be indicated.”

Each vaccine group will consist of about 25 people aged 18-55, and some 25 people aged 56 and older. Three to five months after participants are fully vaccinated, they will receive a single dose of Moderna’s booster vaccine. Additional study arms could be added as vaccines are granted FDA emergency approval or variant-specific vaccines become ready for evaluation, according to the NIH

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