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Clinical Pharmacology In Drug Development

Clinical Pharmacology In Drug Development杂志,由Wiley-Blackwell出版,于2012年创刊,6 issues/year,出版语言English,ISSN:2160-7648,E-ISSN:2160-7648。

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Clinical Pharmacology In Drug Development
Clinical Pharmacology In Drug Development
Clinical Pharmacology In Drug Development
SCI SCIE

杂志介绍

JCR分区
Q3
中科院分区
4区
影响因子
1.7
CiteScore
3.4
期刊收录
SCI、SCIE

Clinical Pharmacology In Drug Development(中文译名:《药物开发中的临床药理学》),ISSN:2160-7648,EISSN:2160-7648,是Wiley-Blackwell出版的国际性学术期刊,创刊于2012年,以6 issues/year形式稳定发行,2026年总发文量约117篇。该刊采用非OA开放访问,学科归属为PHARMACOLOGY & PHARMACY。该刊是医学、药学领域的国际权威刊物,已被SCI(科学引文索引)、SCIE(科学引文索引扩展版)等国际主流学术数据库收录。2026年期刊影响因子达1.7,2025年期刊CiteScore为3.4,2025年期刊自引率约5.9%,在中科院期刊分区体系中位列医学大类4区,在所属学科领域具备高学术影响力与国际认可度。Clinical Pharmacology In Drug Development长期聚焦医学、药学及相关产业的技术应用前沿,在稿件录用评判中,该刊将创新性与前沿性作为核心遴选标准,重点收录能够对医学、药学领域的落地与发展产生实质性推动价值的研究成果。

从全球发文格局来看,USAJapan、CHINA MAINLAND、England、GERMANY (FED REP GER)、Canada、Switzerland等为核心发文国家与地区;GLAXOSMITHKLINEPFIZER、MERCK & COMPANY、ASTRAZENECA、ABBVIE、ASTELLAS PHARMACEUTICALS、JOHNSON & JOHNSON等高校与科研机构是期刊的主要发文单位。

期刊评价

名词解释:

影响因子(Impact Factor, IF):指该期刊前两年发表的文章,在第三年的平均被引用次数。它反映了期刊的近期平均影响力和热度。

中科院分区:中科院分区表是国内主流的学术期刊分级评价工具,核心意义是建立跨学科可比的统一评价标尺,为职称评审、学位授予、科研立项等科研管理工作提供标准化量化依据,同时帮助科研人员筛选优质期刊、规避学术风险,适配国内本土化的科研评价需求。

期刊分区表

《新锐期刊分区表》(2026年3月发布)

大类学科 小类学科 Top期刊 综述期刊
医学
4区
PHARMACOLOGY & PHARMACY 药学
4区

期刊分区表(2025年3月升级版)

大类学科 小类学科 Top期刊 综述期刊
医学
4区
PHARMACOLOGY & PHARMACY 药学
4区

期刊分区表(2023年12月升级版)

大类学科 小类学科 Top期刊 综述期刊
医学
4区
PHARMACOLOGY & PHARMACY 药学
4区

JCR分区

2025-2026年最新版

按JCI指标学科分区 收录子集 分区 排名 百分位
学科:PHARMACOLOGY & PHARMACY SCIE Q3 267 / 356

25.1

学科:PHARMACOLOGY & PHARMACY SCIE Q3 239 / 356

33.01

2023-2024年最新版

按JCI指标学科分区 收录子集 分区 排名 百分位
学科:PHARMACOLOGY & PHARMACY SCIE Q3 265 / 354

25.3

学科:PHARMACOLOGY & PHARMACY SCIE Q3 218 / 354

38.56


中国学者近期发文

1
Bioequivalence and Safety Assessment of Brivaracetam Dry Syrup Compared With Tablets in Healthy Japanese Participants: Results From Two Randomized Single- and Multiple-Dose Trial

Author:Hayakawa, Yoshinobu; Yoshinaka, Ryoji; Sano, Tomonobu; Krauwinkel, Walter; Soma, Tadaharu; Sasamoto, Hiroshi; Elshoff, Jan-Peer; Bass, Almasa; Chen, Ying; Kurihara, Nozomi; Murakami, Harumi

Journal: CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT. 2026; Vol. 15, Issue 4, pp. -. DOI: 10.1002/cpdd.70057

2
Pharmacokinetics, Bioequivalence, and Safety Evaluation of Two Voriconazole Tablets in Healthy Chinese Volunteer

Author:Luo, Pan; Lei, Yongfang; Liu, Chang; Du, Juan; Deng, Xiangxiao; Yu, Hengyi; Qi, Xingxing; He, Zheng; Zhang, Dongling; Zuo, Qin; Fang, Yinian; Liu, Dong; Chen, Qian; Ren, Xiuhua

Journal: CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT. 2026; Vol. 15, Issue 4, pp. -. DOI: 10.1002/cpdd.70058

3
Effect of High-Fat Diet on Pharmacokinetics and Incidence of Adverse Reactions of Tacrolimus in Healthy Chinese Participant

Author:Zhu, Xiufang; Shi, Lingxue; Yang, Lan; Zhang, Nana; Wu, Yujie; Yin, Peihua; Wang, Jianxin; Zhou, Chunhua

Journal: CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT. 2026; Vol. 15, Issue 3, pp. -. DOI: 10.1002/cpdd.70049

4
Pharmacokinetics and Bioequivalence of 2 Deutetrabenazine Tablets in Healthy Chinese Volunteers Under Fasting and Fed Condition

Author:Xu, Dayong; Wang, Pengkai; Li, Yuan; Zhang, Ping; Wei, Liying; Xiong, Xiaolian; Li, Xin

Journal: CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT. 2026; Vol. 15, Issue 3, pp. -. DOI: 10.1002/cpdd.70054

5
A Randomized, Double-Blind, Two-Treatment, Two-Period, Crossover Study Investigating the Systemic Bioavailability of a Novel Cocrystal Ubiquinol Formulation Compared with a Ubiquinone Formulation in Healthy Adult

Author:Mei, Xuefeng; Zhu, Bingqing; Soni, Kshitij; Kasaraneni, Kishore; Panchal, Nirav

Journal: CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT. 2026; Vol. 15, Issue 3, pp. -. DOI: 10.1002/cpdd.70042

6
Pharmacokinetic and Bioequivalence Evaluation of Two Lercanidipine Hydrochloride Tablets in Healthy Chinese Volunteer

Author:Sun, Biao; Zhao, Li; Gan, Fangliang; Zhan, Qiong

Journal: CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT. 2026; Vol. 15, Issue 3, pp. -. DOI: 10.1002/cpdd.70045

7
Pharmacokinetic Characterization and Bioequivalence of Sildenafil Citrate Orally Disintegrating Tablets in Healthy Volunteer

Author:Zhang, Yi; Du, Lijie; Liu, Shirong; Chen, Guiying; Han, Haoran; Huang, Jiangeng; Jiang, Hongliang; Wang, Xiaolu; Guo, Dongsheng; Gan, Fangliang

Journal: CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT. 2026; Vol. 15, Issue 3, pp. -. DOI: 10.1002/cpdd.70041

8
Pharmacokinetic and Bioequivalence Evaluation of Two Repaglinide Tablets Under Fasting and Fed Conditions in Healthy Chinese Volunteer

Author:Sun, Biao; Zhao, Li; Gan, Fangliang; Zhan, Qiong

Journal: CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT. 2026; Vol. 15, Issue 3, pp. -. DOI: 10.1002/cpdd.70044

9
Pharmacokinetics and Safety of VV116 in Subjects With Mild or Moderate Hepatic Impairment Compared With Healthy Controls: A Phase I, Open-Label Stud

Author:Tan, Xi; Lu, Tong; Kuang, Shijuan; Meng, Qin; Yu, Ge; Zou, Jianjun; Wang, Yuya

Journal: CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT. 2026; Vol. 15, Issue 2, pp. -. DOI: 10.1002/cpdd.70037

10
Pharmacokinetics of Aztreonam-Avibactam After Single- and Multiple-Dose Administration: A Phase 1, Open-Label Study in Healthy Chinese Participants and Ethnic Comparison with Non-Chinese Participant

Author:Wang, Jingjing; He, Jinjie; Wu, Jufang; Zhang, Jing; Ma, Ying; Ren, Xiaoqing; Wei, Hua; Zhang, Chunye; Zhu, Hua; Raber, Susan R.; Cong, Shuangchen

Journal: CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT. 2026; Vol. 15, Issue 2, pp. -. DOI: 10.1002/cpdd.70040


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Clinical Pharmacology In Drug Development

国际简称:CLIN PHARM DRUG DEV参考译名:药物开发中的临床药理学

年发文量:117 CiteScore:3.4 是否预警:否 Gold OA文章占比:47.75% 研究类文章占比:99.15%

杂志社联系方式:111 RIVER ST, HOBOKEN, USA, NJ, 07030-5774

Clinical Pharmacology In Drug Development