6月27日，港股次新股药捷安康-B午后拉升，上市一周累涨逾100%！核心产品替恩戈替尼获FDA快速通道认证。
药捷安康近日宣布，其自主研发的多靶点激酶抑制剂替恩戈替尼(TT-00420)，已获美国食品药物管理局(FDA)授予治疗转移性去势抵抗性前列腺癌的快速通道认证。公司表示，替恩戈替尼目前处于全球三期注册实验的多靶点激酶抑制剂，靶向FGFR/VEGFR、JAK和Aurora激酶发挥抗肿瘤作用，目前正在美国与中国进行的临床试验显示，其在多种实体瘤治疗中具有疗效潜力。
招股书显示，药捷安康是一家以临床需求为导向、处于注册临床阶段的生物制药公司，专注于发现及开发肿瘤、炎症及心脏代谢疾病小分子创新疗法。公司的核心产品恩戈替尼(tinengotinib, TT-00420)是一种处于注册临床阶段、自主发现及开发的独特MTK抑制剂，可靶向治疗若干复发或难治、耐药实体瘤。
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