In a press release, Pfizer and its partner BioNTech said the extra shot did the trick, revving up the children's levels of virus-fighting antibodies enough to meet FDA criteria for emergency use of the vaccine with no safety problems.
Preliminary data suggested the three-dose series is 80 per cent effective in preventing symptomatic Covid-19, the companies said, but they cautioned the calculation is based on just 10 cases diagnosed among study participants by the end of April. The study rules state that at least 21 cases are needed to formally determine effectiveness, and Pfizer promised an update as soon as more data is available.
While the vaccine effectiveness likely could change somewhat, "all of this is very positive for those parents who are looking forward to having a vaccine for their younger children in the coming months," said Dr William Moss of the Johns Hopkins Bloomberg School of Public Health, who was not part of the study.
If the FDA confirms the data, the vaccine could "be an important tool to help parents protect their children," agreed Dr Jesse Goodman of Georgetown University, a former FDA vaccine chief. But he cautioned that it's essential to track how long protection lasts, especially against serious disease.
What's next? FDA vaccine chief Dr Peter Marks has pledged the agency will "move quickly without sacrificing our standards" in evaluating tot-sized doses from both Pfizer and Moderna.
Comparing the two companies' approaches to vaccinating the littlest kids promises to be challenging.
Moderna asked the FDA to authorize two shots, each containing a quarter of the dose given to adults. While that spurred good levels of virus-fighting antibodies, Moderna's study found effectiveness against symptomatic Covid-19 was just 40 per cent to 50 per cent during the Omicron surge, much like for adults who've only had two vaccine doses.
"We've learned in older children and adults that ... we really need three doses to get protection" against newer variants like omicron, Moss said.
That's something Moderna plans to study, and Moss said he didn't expect the question would hold up FDA authorization of the first two doses.
Complicating Moderna's progress, the FDA so far has allowed its vaccine to be used only in adults. Other countries allow it to be given as young as age 6, and the company also is seeking FDA authorization for teens and elementary-age kids.
The FDA has tentatively planned for its expert panel to consider Moderna's vaccine for older kids a day before taking up the question of shots for the littlest.
If the FDA clears either vaccine or both, the Centers for Disease Control and Prevention would have to recommend whether all kids under 5 should receive the shots or only those at high risk.
While Covid-19 generally isn't as dangerous to youngsters as to adults, some children do become severely ill or even die. And the Omicron variant hit children especially hard, with those under 5 hospitalised at higher rates than at the peak of the previous delta surge.
It's not clear how much demand there will be to vaccinate the youngest kids. Pfizer shots for 5- to 11-year-olds opened in November, but only about 30 per cent of that age group have gotten the recommended initial two doses. Last week, US health authorities said elementary-age children should get a booster shot just like everyone 12 and older is supposed to get, for the best protection against the latest coronavirus variants.
- AP