Pfizer asks FDA to allow COVID-19 vaccine for children under 5 – NBC Chicago

Pfizer on Tuesday asked the United States to license extremely low doses of its COVID-19 vaccine for children under the age of 5, potentially paving the way for the youngest Americans to start getting vaccinated at the earliest. is in March.

In an unusual move, the Food and Drug Administration urged Pfizer and its partner BioNTech to file earlier than the companies planned.

The country’s 19 million children under the age of 5 are the only group not yet eligible for a vaccine against the coronavirus. Many parents have pushed for the expansion of shots to toddlers and preschoolers, especially as the omicron wave has sent record numbers of babies to hospitals.

With FDA approval, Pfizer injections containing only 1/10 of the adult dose could be dispensed to children under 6 months. Pfizer said Tuesday that it has begun submitting its data to the FDA and expects to complete the process within the next few days.

An open question is how many noses will those children need. Pfizer is testing three shots after two of the ultra-low doses turned out to be potent enough for infants but not enough for preschoolers, and final data from the study is not expected until the end of March. .

That means the FDA could consider whether to allow two shots now, with the possibility of a third shot later if research backs it up.

The FDA said Tuesday it will convene a panel of independent researchers and physicians in mid-February to help review the Pfizer data. The agency is not required to follow the panelists’ advice, but their input is an important step in publicly testing vaccine safety and effectiveness.

Even in the third calendar year of the pandemic, it looks like we continue to fail the COVID test in the hands of Americans – but why? NBCLX narrator Eric Rodriguez examines how the COVID testing infrastructure has changed since March 2020, why omicrons pose so many challenges, and how the testing industry is evolving develop to meet demand.

The FDA’s final decision could be made within a month, but that’s not the only hurdle. The Centers for Disease Control and Prevention was also closed.

The Biden administration has been trying to accelerate the licensing of children’s COVID-19 vaccines, arguing that vaccinations are crucial to opening schools and day care centers and keeping them open. while also freeing parents from childcare duties so they can go back to work. .

However, vaccination rates among children are lower than in other age groups. As of last week, just 20% of children ages 5 to 11 and just over half of 12 to 17 years old had been fully immunized, according to the American Academy of Pediatrics, according to the American Academy of Pediatrics. Nearly three-quarters of adults are fully immunized.

Although young children are at much lower risk of severe illness from coronavirus than adults, it can happen, and COVID-19 infections in children are higher than at any other point in the pandemic.

Dr Sean O’Leary of the University of Colorado, who is on the AAP’s infectious diseases committee, said: “What we’re seeing right now is still a lot of hospitalizations and unfortunately some deaths. death at this age. If the FDA removed vaccinations for these young people, then “that would be really important because all hospitalizations and deaths are essentially preventable.”

Inflammation, stress, memory problems and other symptoms of the “long haul” of COVID-19 are still affecting Fiona Lowenstein and Chimére Smith. Smith told LX News that she developed occipital neuralgia after contracting the virus in March 2020. “It almost felt like I had an elastic band around my head, 20 of them in fact any number of times. any time,” Smith said.

For children younger than 5 years of age, the Pfizer study gave participants two injections three weeks apart, followed by a third dose at least two months later. The company is testing to see if young people produce levels of antibodies similar to those known to protect teenagers and young adults.

In December, Pfizer announced that children under 2 years of age appear to be protected but antibody responses are too low in children aged 2 to 4 years. It’s not clear why, but there is a possibility that the extremely low dose is a bit too low for preschoolers.

Because preliminary results showed the shots were safe, Pfizer added a third dose to the trial, hoping to improve protection.

According to O’Leary, given how effectively boosters work for older age groups, it “may make sense” that younger children could benefit from a third shot. “I can certainly understand where both the company and the FDA are coming from wanting to continue this, in anticipation that there will be a third dose down the line.”

AP journalist Emma H. ​​Tobin contributed. Pfizer asks FDA to allow COVID-19 vaccine for children under 5 – NBC Chicago


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