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		U.S. FDA advisers recommend change to COVID vaccine composition for fall
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		 [June 29, 2022] 
		By Michael Erman and Leroy Leo 
 (Reuters) -Advisers to the U.S. Food and 
		Drug Administration on Tuesday recommended a change in the design of 
		COVID-19 booster shots this fall in order to combat more recently 
		circulating variants of the coronavirus.
 
 The FDA's Vaccines and Related Biological Products Advisory Committee 
		voted 19-2 that the next wave of COVID booster shots should include a 
		component that targets the Omicron variant of the coronavirus.
 
 The FDA plans to decide by early July on what the design of the boosters 
		should be.
 
 FDA scientists at the meeting suggested they preferred vaccines that 
		will target the BA.4 and BA.5 Omicron subvariants that are currently 
		dominant rather than the BA.1 Omicron variant that led to a massive 
		surge in infections last winter.
 
 Dr. Peter Marks, director of the FDA's Center for Biologics Evaluation 
		and Research, said the regulator would hope to launch a booster campaign 
		with a retooled vaccine by October.
 
 
		
		 
		"The better the match of the vaccines to the circulating strain we 
		believe may correspond to improved vaccine effectiveness, and 
		potentially to a better durability of protection," Marks told the 
		meeting of outside expert advisers to the agency.
 
 Pfizer Inc, Moderna Inc and Novavax Inc presented data at the meeting. 
		All three companies have been testing versions of their vaccines updated 
		to combat the BA.1 Omicron variant.
 
 Moderna said it would be ready with a "couple of hundred million" of 
		bivalent, or double targeted, vaccines designed to combat BA.1 by 
		September. It would be late October or early November if it needs to 
		design a vaccine targeting the newer subvariants, the company said.
 
 Pfizer said that it and partner BioNTech already has a significant 
		amount of BA.1 vaccine ready and is preparing to produce a large amount 
		of vaccine targeting BA.4 and BA.5. It said either could be ready for an 
		early October rollout.
 
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			Doses of the Pfizer-BioNTech vaccine against the coronavirus disease 
			(COVID-19) are pictured at a booster clinic for 12 to 17-year-olds 
			in Lansdale, Pennsylvania, U.S., January 9, 2022. REUTERS/Hannah 
			Beier/File Photo 
            
			
			
			 Dr. Kanta Subbarao, representing a 
			World Health Organization advisory committee that also considered 
			the issue, said she preferred BA.1-based vaccines, suggesting they 
			could generate a broader immune response because that variant is 
			more distinct from the original virus than its successor subvariants.
 "Our goal here is to achieve broader immunity against circulating 
			and emerging variants," Subbarao said, noting that trying to match 
			what variant might be circulating in the fall is difficult because 
			of uncertainty about the trajectory of the evolution of the virus.
 
 Both Moderna and Pfizer have said that their respective BA.1 
			inclusive vaccines generated a better immune response against 
			Omicron than their current shots that were designed for the original 
			virus that emerged from China.
 
 They have said their new vaccines also appear to work against BA.4 
			and BA.5, but that protection is not as strong as against BA.1.
 
 The International Coalition of Medicines Regulatory Authorities, a 
			group of global drug regulators that includes the FDA, will meet to 
			discuss the issue on Thursday.
 
 (Reporting by Michael Erman; Additional reporting by Julie 
			Steenhuysen in Chicago and Leroy Leo in Bengaluru; Editing by Bill 
			Berkrot)
 
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