据悉,荣昌生物的核心产品泰它西普近期获得两项重大利好:一是获得欧盟委员会(EC)授予的孤儿药资格认定(Orphan Drug Designation, ODD),用于治疗重症肌无力,成为全球首款同时拥有欧盟和美国孤儿药资格认定的重症肌无力双靶生物制剂;二是获得国家知识产权局授予的专利权期限补偿,补偿天数为1827天,使得该药的专利权期满终止日从2027年6月15日延长到2032年6月15日,为公司核心产品提供额外5年的市场保护。
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