Identification of Drug Characteristics for Implementing Multiregional Clinical Trials Including Japan

被引:5
|
作者
Rokuda, Mitsuhiro [1 ,2 ]
Matsumaru, Naoki [1 ]
Tsukamoto, Katsura [1 ]
机构
[1] Gifu Pharmaceut Univ, Global Regulatory Sci, 1-25-4 Daigakunishi, Gifu 5011196, Japan
[2] Astellas Pharma Inc, Dev, Japan Asia Clin Dev 1, Tokyo, Japan
关键词
agent type; Anatomical Therapeutic Chemical (ATC) code; clinical development; formulation; International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH); multi-regional clinical trial (MRCT); POPULATIONS; STRATEGIES; ANTIBODIES; APPROVAL;
D O I
10.1016/j.clinthera.2017.12.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose: Multiregional clinical trials (MRCT) are a standard strategy used to improve global drug approval efficiency and the feasibility of clinical trials. Japan is the world's third largest drug market with a unique health care system, making it a key inclusion as an operational region for MRCT (MRCT-JP) for global drug development. We aimed to identify the factors required for efficient drug development by comprehensively reviewing the clinical trials of drugs approved in Japan to identify the factors associated with whether or not MRCT-JP is implemented. Methods: We surveyed the review reports and summaries of application data published by the Pharmaceuticals and Medical Devices Agency. We identified drugs for which the clinical trial data package included MRCT-JP and selected the same number of drugs for which the clinical trial data package did not include MRCT-JP from the most recent survey period for comparison. We also examined other publication information, in addition to the review reports, as necessary. The influence of each explanatory variable was analyzed by logistic regression analysis, with whether or not MRCT-JP was implemented as the explanatory variable. Statistical significance was set at 5%. Findings: In the survey period up to September 2017, 165 drugs developed with MRCT-JP were approved for manufacture and sale in Japan. "Respiratory system," "inhalation," "biological drug," and "under review" evaluation status for the United States, European Union, and other areas, "approved" evaluation status for the United States, "new ingredients," "priority review," "non-Japanese firm," and "Top 1-10" and "Top 11-20" drug sales rankings for pharmaceutical companies were identified as potential factors leading to the implementation of MRCT-JP. In contrast, "general anti-infectives for systemic use," "various," "external," "chemical compound," "unsubmitted" evaluation status for both the United States and European Union, and "Top 51+" drug sales rankings were potential factors for not implementing MRCT-JP. (C) 2018 Elsevier HS Journals, Inc. All rights reserved.
引用
收藏
页码:284 / 295
页数:12
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