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舒沃替尼WU-KONG1PartB患者基线情况
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所属报告:
迪哲医药-公司深度报告:小分子创新能力突出商业化前景良好-250617(24页).pdf
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全球范围内已有7款第三代EGFRTKI获批(不包含舒沃替尼)
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2024-09-14
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舒沃替尼治疗EGFR20号外显子插入突变(Exon20ins)患者展现BIC潜力
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2024-09-14
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舒沃替尼治疗经治EGFR20号外显子插入突变患者展现BIC潜力
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行业数据
2024-09-14
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舒沃替尼在EGFRexon20insNSCLC中的临床数据
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其它
2024-07-12
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1L治疗EGFR20号外显子插入突变NSCLC舒沃替尼与竞品药物疗效比较
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2024-04-01
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舒沃替尼二线治疗EGFRex20insNSCLC具有“Best-in-class”竞争力
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2023-11-17
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舒沃替尼单药一线治疗EGFRex20insNSCLCIII期WU-KONG28临床研究方案
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2023-11-17
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根据迪哲医药 2025 年 1 月公告,舒沃替尼在美国用于经治 EGFR Exon20ins NSCLC 的上市申请基于国际多中心注册 II 期临床 WU-KONG1 Part B 研究结果。根据公司于 2024 年 6 月披露的 2024ASCO 数据,截至2024 年 3 月 22 日,107 例纳入疗效分析集患者的初步分析研究结果显示,经 IRC 评估的最佳 ORR 达 53.3%。研究中观察到 3 例患者(2.8%)达到完全缓解(CR),显示治疗的肿瘤缩小深度高,为潜在同类最佳。DoR 未达到,9 个月持续缓解率达 57%。
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迪哲医药-公司深度报告:小分子创新能力突出商业化前景良好-250617(24页).pdf
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舒沃替尼分子式及结构设计亮点
中国EGFRex20insNSCLC新发患者数量
全球EGFRex20insNSCLC新发患者数量
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