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悦康药业:子公司YKYY018雾化吸入剂治疗与预防人偏肺病毒感染的适应症获得FDA临床试验批准
悦康药业公告,全资子公司北京悦康科创医药科技股份有限公司于近日获得美国食品药品监督管理局关于同意YKYY018雾化吸入剂用于人偏肺病毒治疗与预防的临床试验申请的函告,IND编号为180432。YKYY018雾化吸入剂是公司依托全流程AI平台自主开发的一款国际原创的膜融合抑制剂药物,已获得FDA和国家药品监督管理局核准签发的关于用于预防和治疗呼吸道合胞病毒感染进行临床试验的函告。