Article(id=1292126413923045428, tenantId=1146029695717560320, journalId=1246415772164075586, issueId=1292126355785802497, articleNumber=null, orderNo=null, doi=10.13699/j.cnki.1001-6821.2026.04.023, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1768406400000, receivedDateStr=2026-01-15, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1785996543626, onlineDateStr=2026-08-06, pubDate=1772208000000, pubDateStr=2026-02-28, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1785996543626, onlineIssueDateStr=2026-08-06, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1785996543626, creator=13701087609, updateTime=1785996543626, updator=13701087609, issue=Issue{id=1292126355785802497, tenantId=1146029695717560320, journalId=1246415772164075586, year='2026', volume='42', issue='4', pageStart='451', pageEnd='600', issueExtLink='null', onlineDate='null', pubDate='1772208000000', pubDateStr='2026-02-28', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1785996529766, creator='13701087609', updateTime=1786014519902, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1292201811952292026, tenantId=1146029695717560320, journalId=1246415772164075586, issueId=1292126355785802497, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1292201811952292027, tenantId=1146029695717560320, journalId=1246415772164075586, issueId=1292126355785802497, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=594, endPage=600, ext={EN=ArticleExt(id=1292126415634321461, articleId=1292126413923045428, tenantId=1146029695717560320, journalId=1246415772164075586, language=EN, title=Analysis of the characteristics of registered clinical trials of lipid-lowering drugs in China from 2013 to 2025, columnId=1291704889697137247, journalTitle=Chinese Journal of Clinical Pharmacology, columnName=Special Column of Clinical Trials Administration, runingTitle=null, highlight=null, articleAbstract=
Objective

To systematically analyze the longitudinal characteristics and development trends of registered clinical trials of lipid-lowering drugs in China from 2013 to 2025, and to provide evidence-based data for clinical researchers, policy-makers, and pharmaceutical companies.

Methods

Data were retrieved from the National Medical Products Administration (NMPA) Clinical Trial Registration and Information Disclosure Platform. Clinical trials related to lipid-lowering drugs with the first public disclosure date ranging from January 1, 2013 to December 31, 2025 were included. Trials with indications containing keywords such as "cholesterol" and "hyperlipidemia" etc. were screened. After excluding duplicate registrations, comparative analyses were conducted on data regarding basic trial information, drug characteristics and the design of innovative drug trials.

Results

A total of 748 clinical trials were included, of which 68.45% (512 cases/748 cases) were bioequivalence (BE) trials, while phase Ⅰ, Ⅱ, and Ⅲ trials accounted for 125, 47, and 64 trials respectively, totaling 31.55% (236 cases/748 cases). BE trials increased significantly from 2016 to 2019, declined during 2020 to 2022 due to the COVID-19 pandemic, and surged again after 2023. The number of innovative drug trials grew steadily, peaking in 2025. Ninety-four innovative lipid-lowering drugs identified covered diverse therapeutic targets, including proprotein convertase subtilisin/kexin type 9 (PCSK9), angiopoietin-like protein 3 (ANGPTL3), lipoprotein(a) [Lp(a)] and apolipoprotein C3 (APOC3), with 71.28% (67 cases / 94 cases) developed by domestic companies and injections dosage form accounting for 52.13% (49 cases /94 cases). The primary endpoints of phase Ⅲ trials were predominantly the percentage change in low-density lipoprotein cholesterol (LDL-C) from baseline, accounting for 65.52% (38 cases /58 cases), while hard endpoints such as major adverse cardiovascular events (MACE) accounted for only 15.52% (9 cases /58 cases). Target exploration showed a trend of diversification. Novel modalities such as small interfering RNA (siRNA) experienced explosive growth after 2023, with 24 registered trials in 2025. Only 8 innovative drug trials included subjects under 18 years old, all targeting familial hypercholesterolemia.

Conclusion

From 2013 to 2025, China’s lipid-lowering drug clinical trials underwent a critical transformation, shifting from generic drug expansion to active innovative drug research and development. Therapeutic targets have diversified, and novel drug modalities have developed rapidly.

, authors=Qian LI1, Xiao-yuan GUAN1, Di ZHANG2, Ying LOU1, 3, Lei TIAN1, authorsList=Qian LI, Xiao-yuan GUAN, Di ZHANG, Ying LOU, Lei TIAN, authorCompany=null, correspAuthors=Lei TIAN, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1292126415865008182, articleId=1292126413923045428, tenantId=1146029695717560320, journalId=1246415772164075586, language=CN, title=2013-2025年中国降脂药物注册临床试验特征分析, columnId=1291704889869103713, journalTitle=中国临床药理学杂志, columnName=临床试验管理专栏, runingTitle=null, highlight=null, articleAbstract=
目的

系统分析2013~2025年中国降脂药物注册临床试验的纵向特征与发展趋势,为临床研究者、政策制定者及药企提供循证依据。

方法

检索国家药品监督管理局药物临床试验登记与信息公示平台,提取首次公示信息日期在2013年1月1日至2025年12月31日之间的降脂药物相关临床试验,纳入适应症含“胆固醇”及“高脂血症”等关键词的试验,排除重复登记项后,对试验基本信息、药物信息及创新药试验设计等数据进行比较分析。

结果

共纳入748项临床试验,其中68.45%(512项/748项)为生物等效性(BE)试验,Ⅰ、Ⅱ、Ⅲ期试验分别为125、47、64项,合计占比31.55%(236项/748项)。BE试验于2016~2019年增长,2020~2022年受疫情影响回落,2023年后再次迅猛增长;创新药临床试验数量稳步增长,2025年达峰值。94个降脂创新药涵盖前蛋白转化酶枯草溶菌素9(PCSK9)、血管生成素样蛋白3(ANGPTL3)、脂蛋白(a)[Lp(a)]、载脂蛋白C3(APOC3)等多个靶点,其中71.28%(67个/94个)由国内企业贡献,注射剂占比52.13%(49个/94个)。创新药Ⅲ期临床试验主要终点以低密度脂蛋白胆固醇(LDL-C)较基线下降百分比为主,占比65.52%(38项/58项),硬终点主要不良心血管事件(MACE)占比15.52%(9项/58项)。靶点呈多元化拓展趋势,小干扰RNA(siRNA)等新型药物模态于2023年后爆发式增长,2025年siRNA相关试验达24项。受试者含18岁以下人群的创新药临床试验仅8项,均针对家族性高胆固醇血症适应症。

结论

2013~2025年中国降脂药物临床试验实现从仿制药放量到创新药研发活跃的关键转型,靶点布局多元拓展,新型药物模态快速发展。

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李倩(1987-),女,博士,主要从事药物有效性安全性评价方面的研究及工作

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田蕾,研究员,硕士生导师 MP: 13691070380 E-mail:
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2013-2025年中国降脂药物注册临床试验特征分析
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李倩 1 , 管晓媛 1 , 张迪 2 , 娄莹 1, 3 , 田蕾 1
中国临床药理学杂志 | 临床试验管理专栏 2026,42(4): 594-600
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中国临床药理学杂志 |临床试验管理专栏 2026 , 42 (4) : 594 -600
2013-2025年中国降脂药物注册临床试验特征分析
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李倩1, 管晓媛1, 张迪2, 娄莹1, 3, 田蕾1
作者信息
  • 1.中国医学科学院 北京协和医学院 国家心血管病中心 阜外医院 国家心血管疾病临床医学研究中心 国家卫生健康委员会心血管药物临床研究重点实验室,北京 100037
  • 2.清华大学 万科公共卫生与健康学院,北京 100084
  • 3.中国医学科学院 阜外医院 国家心血管病中心 国家心血管疾病临床医学研究中心 Ⅰ期病房,北京 100037
通讯作者:
田蕾,研究员,硕士生导师 MP: 13691070380 E-mail:
作者简介:

李倩(1987-),女,博士,主要从事药物有效性安全性评价方面的研究及工作

Analysis of the characteristics of registered clinical trials of lipid-lowering drugs in China from 2013 to 2025
Qian LI1, Xiao-yuan GUAN1, Di ZHANG2, Ying LOU1, 3, Lei TIAN1
Affiliations
  • 1.NHC Key Laboratory of Clinical Research for Cardiovascular Medications, National Clinical Research Center of Cardiovascular Diseases, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100037, China
  • 2.Vanke School of Public Health, Tsinghua University, Beijing 100084, China
  • 3.National Clinical Research Center for Cardiovascular Diseases, Phase Ⅰ Ward, Fuwai Hospital, Chinese Academy of Medical Sciences, National Center for Cardiovascular Diseases, Beijing 100037, China
出版时间: 2026-02-28 doi: 10.13699/j.cnki.1001-6821.2026.04.023
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目的

系统分析2013~2025年中国降脂药物注册临床试验的纵向特征与发展趋势,为临床研究者、政策制定者及药企提供循证依据。

方法

检索国家药品监督管理局药物临床试验登记与信息公示平台,提取首次公示信息日期在2013年1月1日至2025年12月31日之间的降脂药物相关临床试验,纳入适应症含“胆固醇”及“高脂血症”等关键词的试验,排除重复登记项后,对试验基本信息、药物信息及创新药试验设计等数据进行比较分析。

结果

共纳入748项临床试验,其中68.45%(512项/748项)为生物等效性(BE)试验,Ⅰ、Ⅱ、Ⅲ期试验分别为125、47、64项,合计占比31.55%(236项/748项)。BE试验于2016~2019年增长,2020~2022年受疫情影响回落,2023年后再次迅猛增长;创新药临床试验数量稳步增长,2025年达峰值。94个降脂创新药涵盖前蛋白转化酶枯草溶菌素9(PCSK9)、血管生成素样蛋白3(ANGPTL3)、脂蛋白(a)[Lp(a)]、载脂蛋白C3(APOC3)等多个靶点,其中71.28%(67个/94个)由国内企业贡献,注射剂占比52.13%(49个/94个)。创新药Ⅲ期临床试验主要终点以低密度脂蛋白胆固醇(LDL-C)较基线下降百分比为主,占比65.52%(38项/58项),硬终点主要不良心血管事件(MACE)占比15.52%(9项/58项)。靶点呈多元化拓展趋势,小干扰RNA(siRNA)等新型药物模态于2023年后爆发式增长,2025年siRNA相关试验达24项。受试者含18岁以下人群的创新药临床试验仅8项,均针对家族性高胆固醇血症适应症。

结论

2013~2025年中国降脂药物临床试验实现从仿制药放量到创新药研发活跃的关键转型,靶点布局多元拓展,新型药物模态快速发展。

降脂药物  /  创新药  /  注册临床试验  /  生物等效性试验  /  靶点  /  模态
Objective

To systematically analyze the longitudinal characteristics and development trends of registered clinical trials of lipid-lowering drugs in China from 2013 to 2025, and to provide evidence-based data for clinical researchers, policy-makers, and pharmaceutical companies.

Methods

Data were retrieved from the National Medical Products Administration (NMPA) Clinical Trial Registration and Information Disclosure Platform. Clinical trials related to lipid-lowering drugs with the first public disclosure date ranging from January 1, 2013 to December 31, 2025 were included. Trials with indications containing keywords such as "cholesterol" and "hyperlipidemia" etc. were screened. After excluding duplicate registrations, comparative analyses were conducted on data regarding basic trial information, drug characteristics and the design of innovative drug trials.

Results

A total of 748 clinical trials were included, of which 68.45% (512 cases/748 cases) were bioequivalence (BE) trials, while phase Ⅰ, Ⅱ, and Ⅲ trials accounted for 125, 47, and 64 trials respectively, totaling 31.55% (236 cases/748 cases). BE trials increased significantly from 2016 to 2019, declined during 2020 to 2022 due to the COVID-19 pandemic, and surged again after 2023. The number of innovative drug trials grew steadily, peaking in 2025. Ninety-four innovative lipid-lowering drugs identified covered diverse therapeutic targets, including proprotein convertase subtilisin/kexin type 9 (PCSK9), angiopoietin-like protein 3 (ANGPTL3), lipoprotein(a) [Lp(a)] and apolipoprotein C3 (APOC3), with 71.28% (67 cases / 94 cases) developed by domestic companies and injections dosage form accounting for 52.13% (49 cases /94 cases). The primary endpoints of phase Ⅲ trials were predominantly the percentage change in low-density lipoprotein cholesterol (LDL-C) from baseline, accounting for 65.52% (38 cases /58 cases), while hard endpoints such as major adverse cardiovascular events (MACE) accounted for only 15.52% (9 cases /58 cases). Target exploration showed a trend of diversification. Novel modalities such as small interfering RNA (siRNA) experienced explosive growth after 2023, with 24 registered trials in 2025. Only 8 innovative drug trials included subjects under 18 years old, all targeting familial hypercholesterolemia.

Conclusion

From 2013 to 2025, China’s lipid-lowering drug clinical trials underwent a critical transformation, shifting from generic drug expansion to active innovative drug research and development. Therapeutic targets have diversified, and novel drug modalities have developed rapidly.

lipid-lowering drug  /  innovative drug  /  registered clinical trial  /  bioequivalence trial  /  therapeutic target  /  drug modalitie
李倩, 管晓媛, 张迪, 娄莹, 田蕾. 2013-2025年中国降脂药物注册临床试验特征分析. 中国临床药理学杂志, 2026 , 42 (4) : 594 -600 . DOI: 10.13699/j.cnki.1001-6821.2026.04.023
Qian LI, Xiao-yuan GUAN, Di ZHANG, Ying LOU, Lei TIAN. Analysis of the characteristics of registered clinical trials of lipid-lowering drugs in China from 2013 to 2025[J]. Chinese Journal of Clinical Pharmacology, 2026 , 42 (4) : 594 -600 . DOI: 10.13699/j.cnki.1001-6821.2026.04.023

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doi: 10.13699/j.cnki.1001-6821.2026.04.023
  • 接收时间:2026-01-15
  • 首发时间:2026-08-06
  • 出版时间:2026-02-28
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  • 收稿日期:2026-01-15
基金
作者信息
    1.中国医学科学院 北京协和医学院 国家心血管病中心 阜外医院 国家心血管疾病临床医学研究中心 国家卫生健康委员会心血管药物临床研究重点实验室,北京 100037
    2.清华大学 万科公共卫生与健康学院,北京 100084
    3.中国医学科学院 阜外医院 国家心血管病中心 国家心血管疾病临床医学研究中心 Ⅰ期病房,北京 100037

通讯作者:

田蕾,研究员,硕士生导师 MP: 13691070380 E-mail:
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https://castjournals.cast.org.cn/joweb/zglcylxzz/CN/10.13699/j.cnki.1001-6821.2026.04.023
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2种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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