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昂拉地韦(ZSP1273)II期临床试验主要结果
昂拉地韦(ZSP1273)II期临床试验主要结果
行业数据
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图片格式:PNG
图片大小:480KB
图片尺寸:2310*765
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所属报告:
众生药业-公司深度研究:中药为基稳健增长创新产品打开成长第二曲线-240814(43页).pdf
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Lpa(a)部分管线临床数据整理(注:临床试验预计完成时间以最终公告结果为准)
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行业数据
2026-05-28
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全球各年度生物药临床试验启动数量
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行业数据
2026-05-25
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2025年中国临床试验各类型占比
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行业数据
2026-04-27
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2025年中国临床试验热门靶点竞争格局
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竞争格局
2026-04-27
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参与临床机构试验数量TOP20
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行业数据
2026-04-27
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2025年中国临床试验各药品类型登记量占比
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行业数据
2026-04-27
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2025年中国临床试验登记量TOP10品种
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行业数据
2026-04-27
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2025年中国临床试验热门治疗领域登记数量
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2026-04-27
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2025年中国临床试验申办方TOP20
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2026-04-27
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2026-04-27
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2026-04-27
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2026-04-27
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昂拉地韦片 II 期临床试验表明,与安慰剂相比,不同剂量的昂拉地韦片能显著缩短甲型流感症状缓解时间、缩短发热时间,并加快降低病毒浓度。昂拉地韦片治 II 期临床试验开展了多中心、随机、双盲、安慰剂对照试验,共入组 172 例研究对象为急性无并发症的中国成年甲型流感患者,受试者被随机分为四组(1:1:1:1):昂拉地韦 200mg 每日两次(BID)、400mg 每日两次(BID)、600mg每天一次(QD)或匹配的安慰剂,疗程 5 天。主要疗效指标是意向治疗(ITT)人群中七项流感症状(咳嗽、咽痛、头痛、鼻塞、发热或寒颤、肌肉或关节痛和疲劳)缓解时间和缩短发热时间,并能快速降低和清除体内流感病毒)持续缓解的时间(TTAS)结果显示:所有昂拉地韦组的 TTAS 中位时间均降低(安慰剂组 62.87小时 vs 昂拉地韦组 200mg/400mg/600mg 组:46.92/54.87/40.05 小时;所有昂拉地韦组的中位退烧(腑温<37℃)时间均明显短于安慰剂组(安慰剂组 60.27小时 vs 昂拉地韦组 200mg/400mg/600mg 组 31.93 小时/25.33 小时/23.88 小时),并且昂拉地韦缩短了病毒浓度可测持续时间(安慰剂组 71.85 小时 vs 昂拉地韦组 200mg/400mg/600mg 41.95/62.26/41.77 小时)。最常见的 AE 是腹泻(40.94%);本研究未观察到严重不良反应。
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