The FDA plans to “follow the science” with eyes on COVID-19 vaccines for children younger than 12 as schools begin to get back in session around the country, the agency said in a news release attributed to acting Commissioner Dr. Janet Woodcock and Dr. Peter Marks, director of the FDA’s Center for Biologics Research and Evaluation.
“As regulators, we recognize we have an important task ahead of us that will require us to act expeditiously while undertaking an extremely meticulous and thoughtful review once we receive requests to authorize a COVID-19 vaccine for emergency use or submissions for approval of a COVID-19 vaccine for this population,” the FDA said in the news release.
“Children are not small adults — and issues that may be addressed in pediatric vaccine trials can include whether there is a need for different doses or different strength formulations of vaccines already used for adults.”
“When it comes to immunosuppressive agents in dermatology, there are several different medications and all portend their own risk. Any immunosuppressive medication choice and subsequent use should be viewed in the light of the risk and benefits, including the severity of the skin disease the medication is being prescribed to treat,” Humphrey said.
In terms of potential COVID-19 vaccines for younger children, the FDA has outlined the steps it plans to take in order to ensure safety and efficacy in vaccines for children as vaccine manufacturers have reported that the necessary clinical trials involving children as participants are currently underway.
Those trials are expected to include a follow-up period of at least about two months, allowing for the proper safety monitoring following the administration of vaccine doses for at least half of the clinical trial vaccine recipients.
Once those trials are completed, the FDA will work closely with each manufacturer to ensure that the analysis of the data from the studies is robust and meets regulatory standards, after which the manufacturers will compile the information and potentially request emergency use authorization (EUA) or submit for approval a biologics license application (BLA) to the FDA.