“一针抵得上一套豪宅”的药价，正从科幻想象逐步走向现实。 11月24日，诺华公司宣布，美国食品和药物管理局（FDA）已批准Itvisma（onasemnogene abeparvovec）用于治疗年满两岁及以上、已确诊携带运动神经元存活基因1（SMN1）基因突变的脊髓性肌萎缩症（SMA）儿童、青少年及成人患者。 根据公开信息，Itvisma的活性成分与诺华脊髓性肌萎缩基因疗法Zolgensma...
Source Link“一针抵得上一套豪宅”的药价，正从科幻想象逐步走向现实。 11月24日，诺华公司宣布，美国食品和药物管理局（FDA）已批准Itvisma（onasemnogene abeparvovec）用于治疗年满两岁及以上、已确诊携带运动神经元存活基因1（SMN1）基因突变的脊髓性肌萎缩症（SMA）儿童、青少年及成人患者。 根据公开信息，Itvisma的活性成分与诺华脊髓性肌萎缩基因疗法Zolgensma...
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