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舒沃替尼临床开发历程
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所属报告：
迪哲医药-公司研究报告-迪行小分子赛道折桂全球创新之巅-250126（44页）.pdf
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行业数据
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EGFRExon20ins新兴疗法：莫博赛替尼撤市，舒沃替尼、埃万妥获批，伏美替尼在研
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行业数据
2025-03-07
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舒沃替尼结构式与作用机制
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行业数据
2025-02-06
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舒沃替尼季度销售（万元）
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行业数据
2025-02-06
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赛沃替尼临床开发进度（截至24.7.1更新）
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行业数据
2025-01-24
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赛沃替尼vs竞品：治疗EGFR-TKI耐药NSCLC的疗效及安全性
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行业数据
2024-12-31
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赛沃替尼vs竞品：pRCC疗效及安全性
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行业数据
2024-12-31
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赛沃替尼NSCLC适应症销售预测（国内）
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行业数据
2024-12-31
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赛沃替尼：销售预测（海外）
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行业数据
2024-12-31
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临床开发速度高效，美国商业化即将开启：舒沃替尼自进入临床开发阶段以来，连续三年在 ASCO、WCLC、ESMO 等国际顶级学术大会亮相并斩获三项口头报告。从国内首例临床研究受试者入组到正式获批上市，仅 4 年不到时间，突破了肺癌靶向药物临床开发新速度。海外临床试验推进速度也很快，25 年 1 月美国 NDA 受理并授予了优先审评资格，我们预计 2025H2 有望实现美国获批上市。作为中国自主研发的首款针对EGFR Exon20 ins 突变的肺癌靶向药，舒沃替尼是公司高效源头创新的最好证据，也体现了公司临床开发团队的高效和高标准。
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迪哲医药-公司研究报告-迪行小分子赛道折桂全球创新之巅-250126（44页）.pdf
2018-2024Q1-Q3公司研发投入（百万元）
2021-2024Q1-Q3研发人员数量（人）
2020-2024Q1-Q3的现金及现金等价物（百万元）
舒沃替尼季度销售（万元）
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