7月25日,药捷安康-B午后涨近13%,创上市新高。
消息面上,药捷安康本月初宣布,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。
光大证券国际此前发布研报称,由于创新疗法(包括FGFR抑制剂)的市场渗透率预期会增加,CCA的市场规模的年复合增长率预期会高于发病率。国元国际则表示,公司在细分行业研发领先,替恩戈替尼是全球首个且唯一进入注册临床阶段用于治疗复发或难治性胆管癌患者的FGFR抑制剂。它也是全球首个可能同时抑制FGFR/JAK通路并针对转移性去势抵抗性前列腺癌具有临床疗效证据的研究药物。
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