Professor John Skerritt said the medical regulator will “dig even deeper” on the data before approving the vaccine for young children.Credit:Alex Ellinghausen
“As soon as any medicine or vaccine is proposed for use,or applied for use,in children,you need to dig even deeper,” Professor Skerritt said.
“We look at safety very thoroughly for every age group. But we dig even deeper for children. The trial data for children will be on more kids[than there was for] the booster,safety monitoring will be for a longer period.”
The TGA received a partial application from Pfizer on Tuesday to provide its vaccine to children aged five to 11. Professor Skerritt said the regulator expected to receive the remaining data in the next fortnight.
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“We still have more to get from the Pfizer application for five to 11-year-olds,” he said on Wednesday morning.
“I would hope that we would get there by the end of November,but it really does depend on when we get the full application from Pfizer,the complete version,and if there are any issues,” he said.
The US has also moved a step closer to approving the vaccine for young children after a Food and Drug Administration advisory panel agreed that thevaccine’s benefits outweighed potential risks.