美国药厂辉瑞在周五表示,其新冠疫苗在临床试验中,显示5至11岁儿童接种后,有效率达90.7%。
有2268名儿童参与是次临床试验,其中约三分之二的儿童接种每针10微克的疫苗,剂量是成人的三分之一;其余儿童则接种安慰剂,两针间隔3周。结果显示,接种低剂量疫苗的群组中,有3人感染新冠;至于安慰剂群组则有16人染疫,推算出疫苗的有效率接近91%,两个群组均无重症报告,但接种疫苗者的症状比未接种者更轻。
辉瑞表示,已将报告呈交予食品及药物管理局(FDA),而FDA的专家会在下周二表决是否向5至11岁群组推荐注射该疫苗,预计在下月初会有最终决定。
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