7月7日，KalVista Pharmaceuticals今日宣布，美国食品药品监督管理局 (FDA) 已批准 EKTERLY (sebetralstat)，这是一种新型血浆激肽酶抑制剂，用于治疗12岁及以上成人和儿童患者的遗传性血管水肿 (HAE) 的急性发作。EKTERLY 是治疗 HAE 的首个也是唯一的按需口服治疗。受此消息提振，KalVista Pharmaceuticals美股盘中飙涨逾18%。
7月7日，KalVista Pharmaceuticals今日宣布，美国食品药品监督管理局 (FDA) 已批准 EKTERLY (sebetralstat)，这是一种新型血浆激肽酶抑制剂，用于治疗12岁及以上成人和儿童患者的遗传性血管水肿 (HAE) 的急性发作。EKTERLY 是治疗 HAE 的首个也是唯一的按需口服治疗。受此消息提振，KalVista Pharmaceuticals美股盘中飙涨逾18%。
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