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安罗替尼已获批适应症(截至2025年7月20日)
安罗替尼已获批适应症(截至2025年7月20日)
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所属报告:
中国生物制药(1177.HK)-港股公司研究报告:创新管线价值重估制药龙头华丽转身-250731(76页).pdf
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瑞康曲妥珠单抗与德曲妥珠单抗2LNSCLC适应症和数据对比(非头对头)
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2026-05-28
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瑞康曲妥珠单抗销售预测(仅限肺癌适应症)
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2026-05-28
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表10、国内“肤质改善”适应症,合规械三水光盘点
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2026-05-11
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全球肝癌药物适应症TOP10
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行业数据
2026-04-30
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中国肝癌药物适应症TOP10
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行业数据
2026-04-30
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瑞康曲妥珠单抗与德曲妥珠单抗2LNSCLC适应症和数据对比(非头对头)
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行业数据
2026-04-20
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瑞康曲妥珠单抗在研适应症(截至2026年2月)
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行业数据
2026-04-20
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全球范围临床阶段ASI高血压适应症在研情况(截至2026年3月25日)
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行业数据
2026-04-01
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全球ETAR拮抗剂-高血压适应症临床阶段在研格局(截至2026年3月25日)
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竞争格局
2026-04-01
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ETA靶向药肾病适应症研发格局(截至2026年3月26日)
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值得注意的是,安罗替尼联合贝莫苏拜单抗、卡铂和依托泊苷一线治疗广泛期小细胞肺癌 (ES-SCLC) 的适应症参加了 2024 年 10 月进行的国家医保谈判,但最终此适应症并没有纳入医保。我们认为,优异的临床数据是公司的信心来源,III 期临床试验(CTR20192538)显示,安罗替尼联合贝莫苏拜单抗、卡铂和依托泊苷治疗的广泛期小细胞肺癌患者的中位无进展生存期(mPFS)和中位总生存期(mOS)分别为 6.9 个月和 19.3 个月,显著高于化疗对照组的 4.2 个月和 11.9 个月,mPFS 和 mOS 的 HR(hazard ratio, 风险比)分别为0.32 和 0.61。此项临床试验是 VEGF+免疫疗法联合化疗在广泛期小细胞肺癌治疗上的首次成功,也是目前 mPFS 和 mOS 最长的治疗方案。
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中国生物制药(1177.HK)-港股公司研究报告:创新管线价值重估制药龙头华丽转身-250731(76页).pdf
治疗肥胖的临床数据比较(治疗52周)
中国生物制药经调整净利润预测
中国生物制药EBITDA预测
中国生物制药研发费用率预测
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