康缘药业KYS202004A注射液获FDA临床试验批准

财中社11-08

财中社11月8日电康缘药业（600557）发布关于KYS202004A注射液获得美国FDA临床试验批准的公告。公司近日收到FDA的函件，同意其针对银屑病的临床试验申请。KYS202004A注射液是公司自主研发的双靶点Fc融合蛋白，拥有独立完整的知识产权，至今累计研发投入约8810万元。此外，该药品已获得中国国家药品监督管理局的药物临床试验批准通知书。公告中提到，尽管临床试验及审批结果存在不确定性，...

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