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2LSCLC化疗临床数据对比(非头对头)
2LSCLC化疗临床数据对比(非头对头)
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所属报告:
绿叶制药-港股公司研究报告-主营业务稳健增长多款新药进入商业化兑现阶段-240129(32页).pdf
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相关数据
在研阶段的ADC产品在2LSCLC与3LSCLC均有所布局,初步临床数据已展现出了较好的疗效
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行业数据
2025-05-13
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吉利德正在开展戈沙妥珠单抗与Topotecan针对2LSCLC的头对头III期临床试验
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行业数据
2025-05-13
原图定位
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Ifinatamabderuxtecan正在2LSCLC中开展与标准疗法托泊替康或者芦比替定的头对头III期临床试验
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行业数据
2025-05-13
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HS-20093正在2LSCLC中开展与标准疗法Topotecan的头对头III期临床试验
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2025-05-13
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芦比替丁治疗2LSCLC患者mOS达9.7个月(CTFI指无化疗间隔)
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行业数据
2024-09-14
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不1LSCLC疗法临床试验结果对比
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芦比替定于 2020年在美国食品药品监督管理局(FDA)获得加速批准,用于治疗在含铂类化疗过程中或化疗后出现疾病进展的转移性 SCLC 成年患者,成为近二十七年来首个获得美国 FDA批准的用于治疗复发性 SCLC的新分子实体。该获批主要基于芦比替定的一项单药治疗 105例接受铂类药物化疗后出现疾病进展的 SCLC成年患者(包括铂类敏感和耐药患者)的开放标签、多中心、单臂、II期篮试验。研究结果显示:接受芦比替定治疗的患者总有效率(ORR)达到 35%,中位缓解持续时间(DoR)为 5.3个月,中位总生存期(OS)为 9.3个月。其中,芦比替定在化疗敏感型患者群体(停疗至复发间隔(CTFI)≥90 天)中的单药疗效 ORR 可达 45%,中位 OS可达 11.9个月。和拓扑替康、氨柔比星(化疗)及纳武尤利单抗(PD-1)等相比,显示出患者在总生存期(mOS)最长获益。
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