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KEYNOTE-024于2016ESMO公布的初步临床结果
KEYNOTE-024于2016ESMO公布的初步临床结果
行业数据
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图片格式:PNG
图片大小:303KB
图片尺寸:2310*1025
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所属报告:
医药行业专利系列研究(一):K药、O药专利纠纷全梳理-230719(21页).pdf
打包全文图表
相关数据
ESMO大会中国LBA翻三倍,多款重磅新药亮相
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行业数据
2025-10-23
原图定位
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国内药企入选2025ESMO大会LBA摘要情况
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行业数据
2025-10-23
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2025-09-18
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2025-09-18
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图16.LAE002在2024年ESMO大会上展示临床结果
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2025-06-30
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2025-05-15
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其它
2024-07-10
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其它
2024-07-10
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KEYNOTE-042研究:疗效终点(5年随访)
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2024-06-27
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KEYNOTE-042研究:PD-L1TPS≥1%患者的PFS(3年跟踪)
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2024-06-27
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KEYNOTE-024研究:生存期获益(5年随访)
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2024-06-27
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图232030ESMO晚期乳腺癌诊疗指南
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2024-05-23
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2021ESMO大会JUPITER-06研究最终OS分析数
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2023-12-19
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2021ESMO大会JUPITER-06研究最终PFS分析
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2023-12-19
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2023ESMO临床研究企业分布
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2023-10-26
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2016 年 10 月 9 日,也即 O 药 NSCLC 一线治疗 III 期临床实验失败两个月后,默沙东的 KEYNOTE-024 实验初步结果于 2016 年 ESMO 大会上公布,初步结果显示 K 药组患者相比化疗组患者,其 PFS 延长了近 4 个月(10.3 个月 vs 6.0个月);尽管 OS 数据尚不成熟,但仍能观测到 K 药组患者生存获益延长;ORR 方面,K 药组与化疗组分别为 45%与 28%,且 K 药缓解时间更长,副作用更低。
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医药行业专利系列研究(一):K药、O药专利纠纷全梳理-230719(21页).pdf
纳武利尤单抗中国获批的癌症/瘤种领域梳理
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帕博利珠单抗中国获批的癌症/瘤种领域梳理
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