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腾讯网
1 个月
优于标准疗法!诺华一线抗癌突破性小分子疗法再获FDA批准
诺华(Novartis)日前宣布,美国FDA加速批准Scemblix(asciminib)用于治疗新确诊的费城染色体阳性慢性髓系白血病慢性期(Ph+ CML-CP)成人患者。根据 ...
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16 天
FDA 加速批准 Scemblix 治疗慢性期新诊断的 Ph+ CML
美国食品药品管理局(FDA)已加速批准 Scemblix ®(asciminib),用于治疗新诊断的费城染色体阳性慢性粒细胞白血病(Ph+ CML)慢性期(CP)成人患者。
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Trump warns BRICS nations
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Ukraine seeks NATO invite
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UK spy chief accuses RU
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Canadian media outlets sue
Little Rock mall shooting
Chiefs clinch playoff berth
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