That may seem ploddingly slow, given that Pfizer-BioNTech’s young children, who “are not just little adults,” says Dr. William Towner, physician director of for the Kaiser Permanente Department of Research & Evaluation in Southern California.. (Moderna submitted its shot for authorization among adolescents and teenagers in June, but the FDA hasn’t decided yet.) But the research process is different for
One significant difference: 12- to 15-year-olds received the sameas adults, whereas researchers have had to figure out the right amount to give to younger children. With smaller bodies—and that seem better prepared to fight off COVID-19—young kids should bee to get strong protection ler dose, hopefully, with fewer side effects, French explains.
After landing on the proper doses for kids, trial sites moved into safety and efficacy testing, starting with children ages 5 to 11 and then. That process is ongoing, and it was disrupted when the FDA in asked researchers testing both the Pfizer-BioNTech and Moderna vaccines to enroll additional children in their trials, in hopes of learning more about whether rare side effects, like heart conditions seen in a small number of teenagers after vaccination, also affect younger kids.
Both Pfizer and Moderna are still recruiting participants for at least some of their study sites, but reaching that higher enrollment cap shouldn’t be a problem, Towner says. Kaiser Southern California is one of the sites across the country testing Moderna’syounger than 12—and the owner says he receives at least 1tenapplications from eager parents for each trial spot that opens up. “There’s d strong interest in this clinical trial,” Towner . “We’ve been getting a rather breathtaking response.”
Even still, authorization for 5- to 11-year-olds is likely at least a few months off, French guesses. Before granting emergency-use authorizations for adult and, the FDA reviewed two months of follow-up safety data from trial participants. It’s likely to want at least that much data from pediatric trials and perhaps more. An FDA spokesperson referred TIME to agency it will review at least two months of data for kids.
In a statement to TIME, a Pfizer spokesperson said that the company expects to have enough data to potentially support an emergency-use authorization for 5- to 11-year-olds by the end of September. Moderna representatives did not provide a statement before press time. Dr. Kari Simonsen, leading Omaha Children’s Hospital and Medical Center’s pediatric trial of the , says she feels two months of follow-up is enough. “As a pediatrician, I feel like using that same rationale that we did for adolescents and adults makes good sense,” Simonsen says. Her Nebraska hospital has already enrolled and participants and is waiting for the FDA’s signal to advance. “It’s . “I’m just anxiously awaiting when I’ll take that up.”
Many parents can’t wait for that day, as evidenced by the overwhelming response research centers nationwide have gotten to their recruitment requests. That anticipation was seemingly only heightened when Pfizer-BioNTech’sin August. In fact, after that approval, the American Academy of Pediatrics (AAP) issued a off-label for children, apparently anticipating the wishes of concerned parents. “We do not want individual physicians to be calculating doses and dosing schedules one-by-one for younger in older patients,” Dr. Yvonne Maldonado, chair of the AAP committee on , said in the statement.
“We should do this based on all of the evidence for each age group; for that, we need the trials to bd. I know parents are anxious to protect their children, but we want to ensure children benefit from ongoing clinical trials.” Even as some parents count down the days until pediatric shots are available. However, an even larger group remains skeptical. An international study published in November 2020 found that just 18% of parents trial. And in an August 2021 Kaiser Family Foundation survey, only 26% of U.S. with kids ages 5 to 11 said they would vaccinate them immediately. Forty percent said they would “wait and see,” w% said they would vaccinate their kids only if required, and 25% said they wouldn’t under any circumstances.
Dr. Kelly Moore, president and CEO of the pro-vaccine Immunization Action Coalition says pediatricians should start counseling parents about the benefits of vaccination as soon as possible, even though shots aren’t authorized for young kids yet. “Families are used to looking to their pediatrician for guidance on what happens to their child,” Moore says. “More than ever, the pediatrician’s ability to educate families is going to be critical.” Schools wilwillShe says schools will have ole, particularly for kids who may not have regular interactions with providers. o urges parents to pay attention to current pediatric and Midwest and to use that when making decisions about vaccination and other precautions. “We can show you that kids are getting sick, we can show you that kids are getting hospitalized, we can show you that kids are dying,” he says. “Please use that data.”