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T2DM:III期临床试验结果——安全耐受
T2DM:III期临床试验结果——安全耐受
行业数据
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图片格式:PNG
图片大小:179KB
图片尺寸:1889*822
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所属报告:
君圣泰医药~B-港股公司研究报告-HTD1801发力代谢疾病市场-250527(26页).pdf
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全球I-III期临床试验启动数量(2016-2025年)
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行业数据
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图D.附录III.RRF对荷兰的数字溢出效应:按原产国划分的贡献
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图C.附录III.RRF对德国的数字溢出效应:按原产国划分的贡献
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图表9截至2026年5月国内外脑机接口临床试验统计
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行业数据
2026-05-28
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全球主要在研CLDN18.2ADC产品(II/III期)
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行业数据
2026-05-28
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PCSK9药物研发格局(筛选全球最高研发阶段进入III期的活跃管线)
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竞争格局
2026-05-28
原图定位
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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
原图定位
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CDK4/6i耐药HR+乳腺癌III期阶段以后在研品种(最高研发阶段开始日期在2023年及以后)
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行业数据
2026-05-11
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各线食管鳞癌的在研创新药格局梳理(III期及申请上市阶段)
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竞争格局
2026-05-11
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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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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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行业数据
2026-04-27
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两项研究中,根据公司公开的数据,HTD1801 皆表现出良好的安全性和耐受性,最常见的不良事件是胃肠道不良反应,与之前临床研究结果一致。可能因不良事件停药的受试者少于 2%。未见明显低血糖风险。从临床结果来看,服用 HTD1801 甚至可以降低患者的不良反应,发生不良反应的比例低于安慰剂组。
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君圣泰医药~B-港股公司研究报告-HTD1801发力代谢疾病市场-250527(26页).pdf
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HTD1801通过多重机制维持代谢稳态
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