Pfizer and BioNTech said on Monday that preliminary findings of a clinical trial of children younger than five showed three doses of their coronavirus vaccine produced a strong enough immune response to meet the criteria for regulatory authorization.
In a news release, the companies announced results from a subset of a trial of 1,678 children ages 6 months through 4 years, saying the three-dose regimen had been 80 percent effective in preventing symptomatic infection. No supporting data was disclosed, and the companies did not say how many children were in the subset. A spokeswoman for Pfizer said comprehensive results from the trial will be disclosed next month.
Both Pfizer and Moderna are hoping to soon win authorization to vaccinate the nation’s youngest children. About 18 million children under the age of 5 are the only Americans not yet eligible for vaccination against the coronavirus, and parents’ expectations for when shots will be offered have been repeatedly dashed.
Pfizer and its partner BioNTech said the number of children in the trial who fell ill with Covid was too small to make a definitive statement on efficacy. Only 10 children participating in the trial became ill with Covid after those in the vaccination group were given the third dose. The clinical trial’s protocol specified that analysis of vaccine efficacy required at least 21 Covid cases. The companies said that final data on efficacy, a secondary endpoint for the clinical trial, would be shared “once available.”
The Biden administration had hoped to offer vaccine doses to those under 5 as early as February. The Food and Drug Administration initially pressed Pfizer to submit data on how well two doses worked for young children, but pulled back after Pfizer said two doses were not sufficiently effective in preventing symptomatic infection from the highly contagious Omicron variant.
But Pfizer said that the new results showed that three doses, with the third given at least two months after the second, stimulated the immune system to strongly protect against the virus, with no safety concerns. Researchers said the immune response of the subset of trial participants, measured one month after the third dose, compared favorably to that of people 16 to 25 who received two doses.
“We are pleased that our formulation for the youngest children, which we carefully selected to be one-tenth of the dose strength for adults, was well tolerated and produced a strong immune response,” Dr. Albert Bourla, Pfizer’s chief executive, said in a statement. Dr. Ugur Sahin, chief executive of BioNTech, said the companies would complete their F.D.A. application for emergency authorization of the pediatric vaccine this week.
The new findings heat up a competition between Moderna and Pfizer over which company will produce the best vaccine for the youngest Americans. Moderna is proposing a two-dose regimen for children younger than 6, using a quarter the strength of its adult dose. The company has said it anticipates that a third dose will be necessary as a booster shot, but it has not yet submitted any data on that to the government.
The question of which vaccine works better will be at least indirectly put before a committee of outside advisers to the F.D.A., at a meeting scheduled for June 15. With both Pfizer and Moderna proposing different dosing regimens for the youngest children and presenting different clinical trial results, the committee will consider whether each vaccine meets the requirements for emergency use authorization.
In late April, Moderna sought emergency authorization of its pediatric vaccine after interim results showed that clinical trial participants had a similar immune response to young adults when given a dose one-fourth as strong.
Like Pfizer, the firm said its results met the clinical trial criteria for success. Moderna has said its vaccine appeared to be 51 percent effective against symptomatic infection among children younger than 2, and 37 percent effective among those 2 to 5.
If Pfizer’s results are borne out by subsequent data, its efficacy would be better than Moderna’s. Both companies say their vaccines produce similar side effects to other pediatric vaccines that have been used for decades.
On June 14, the F.D.A.’s outside experts will discuss the Moderna vaccine for children and adolescents from 6 to 17 years.
Adeel Hassan contributed reporting.
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