

September 29, 2021, (Reuters) – Pfizer Inc (PFE.N) and BioNTech SE on Tuesday submitted initial trial data for their COVID-19 vaccine in 5 to11 year olds and said they would make a formal request to U.S. regulators for emergency use in the coming weeks.
The U.S. Food and Drug Administration said earlier this month it would look to complete its data review for this age group as quickly as possible, likely in a matter of weeks rather than months. That could mean an authorization of the shot for children by the end of October, sources have told Reuters.
The companies, however, have yet to start the official process for authorization, which could slow the decision. According to the Wall Street Journal, the FDA may not make its decision until sometime between Halloween and Thanksgiving, citing a person familiar with the matter.
A Pfizer spokesperson said the company expects to start and complete its application very soon.
A decision on the vaccine’s use in younger children is eagerly awaited by millions of Americans as coronavirus infections have soared in children to the highest point in early September, according to data from the American Academy of Pediatrics.
The vaccine, which is already authorized for 12 to 15-year- olds and fully approved for ages 16 and up, induced a strong immune response in the target age group in a 2,268-participant clinical trial, the companies said on Sept. 20. read more
The Pfizer-BioNTech vaccine was authorized for the 12-15 age group roughly a month after the companies filed for authorization. If the same timeline is followed for this application, younger children could start receiving their shots as soon as late October.
A rapid authorization could help mitigate a potential surge of cases this fall, with schools already open nationwide.
While kids are less susceptible to severe COVID-19, they can spread the virus to others, including vulnerable populations that are more at risk of severe illness.
The companies said they plan to submit the data to the European Medicines Agency and other regulatory authorities. They also plan to submit data from the full late-stage trial for scientific peer-reviewed publication.
The FDA was not immediately available to comment.
Data from the companies’ trial showed the two-shot vaccine generated an immune response in children that matched what was previously observed in 16-to-25 year olds. The safety profile was also comparable to the older age group, Pfizer said.
The drugmakers are also testing the vaccine in children aged 2-to-5 and those aged 6 months-to-2 years, with data expected in the fourth quarter.
Moderna’s (MRNA.O) COVID-19 vaccine is not yet authorized for use in adolescents in the United States, while it has gained authorization for that age group in Europe.
Both the Pfizer and Moderna vaccines have been linked by regulators to rare cases of heart inflammation in adolescents and young adults, particularly young men. Pfizer said no instances of heart inflammation were seen in the trial participants.
Source: Reuters
more recommended stories
4 National Guard officers imprisoned for human trafficking with migrants in Oaxaca
OAXACA, Oaxaca, March 29, 2023.- Four.
Panic after shooting outside a school in Morelos
CUERNAVACA, Mor., March 29, 2023.- A.
ARVAY promotes gastronomy from Valladolid in the United States
San Diego, California, March 28, 2023.-.
Vila promotes Yucatan’s port development at the most important international cruise fair
Vila Dosal held working meetings with.
Yucatan State government suffers a cyberattack: DMV module without “system”
The license plate and driver’s license.
UADY’s project will link Yucatan and Cuba
Yucatan and Cuba join academic efforts.
Land with ancient Mayan civilization buildings commercialized in Yucatán
Unbelievable, but true. In a Facebook.
Two of the most important companies in the world: Microsoft and FedEx ready to invest in Yucatán
In the early hours of this.
More than 30 migrants from India detained in Yucatán
March 28.- The Secretariat of Public.
National Queso de Bola and Panucho Festival in Yucatán
On April 1st and 2nd, the.
Leave a Comment