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美国、英国和日本世界卫生组织儿童基本药物的批准状况与证据:一项横断面研究。

Approval status and evidence for WHO essential medicines for children in the United States, United Kingdom, and Japan: a cross-sectional study.

作者信息

Shimazawa Rumiko, Ikeda Masayuki

机构信息

Department of Clinical Pharmacology, Tokai University School of Medicine, 143 Shimokasuya, Isehara, Kanagawa 259-1193 Japan.

Department of Medical Informatics, Kagawa University Hospital, Miki-cho Ikenobe, Kagawa 761-0793 Japan.

出版信息

J Pharm Policy Pract. 2017 Jan 6;10:4. doi: 10.1186/s40545-016-0094-2. eCollection 2017.

Abstract

BACKGROUND

The WHO Model List of Essential Medicines for Children (EMLc) covers medicines for globally high-burden diseases. Regulatory approval in high-income countries ensures evidence and dosage form but usually focuses on diseases common in those countries and not in low- and middle-income countries.

METHODS

This cross-sectional study assessed supporting evidence for the 346 medicines in the 5th WHO EMLc and their approval data from the United States, United Kingdom, and Japan.

RESULTS

Of the 346 EMLc medicines, 307 were approved in one or more of the three countries, 278 of which had supporting evidence of efficacy. The percentage of medicines approved in one or more of the three countries was lowest for antiparasitics (60%) whereas 100% for medicines for cancers and musculoskeletal and respiratory conditions were approved. Five of the 30 EMLc antineoplastics had no supporting paediatric evidence. Of the 39 EMLc medicines unapproved in all three countries, 26 were indicated for neglected infectious diseases (NIDs). Ten of the 26 had supporting paediatric evidence. Seventeen of the 39 unapproved medicines had no paediatric dosage form available, and all 17 were indicated for NIDs.

CONCLUSIONS

Most EMLc medicines for diseases common in the three countries had supporting evidence, which was closely associated with approval, whereas a substantial number of medicines for NIDs were unapproved in the three countries, regardless of whether they had supporting evidence. Because of the limited contribution to the EMLc from high income countries, appropriate incentive mechanisms for pharmaceutical companies are required to make paediatric development for NIDs feasible and effective.

摘要

背景

世界卫生组织儿童基本药物示范清单(EMLc)涵盖了全球高负担疾病的药物。高收入国家的监管批准确保了证据和剂型,但通常侧重于这些国家常见的疾病,而非低收入和中等收入国家常见的疾病。

方法

这项横断面研究评估了世界卫生组织第5版EMLc中346种药物的支持证据及其来自美国、英国和日本的批准数据。

结果

在346种EMLc药物中,307种在这三个国家中的一个或多个国家获得批准,其中278种有疗效支持证据。在这三个国家中的一个或多个国家获得批准的药物百分比,抗寄生虫药物最低(60%),而癌症、肌肉骨骼和呼吸系统疾病的药物获批率为100%。30种EMLc抗肿瘤药物中有5种没有儿科支持证据。在所有三个国家均未获批的39种EMLc药物中,26种用于被忽视的传染病(NIDs)。26种中有10种有儿科支持证据。39种未获批药物中有17种没有儿科剂型,且所有17种均用于NIDs。

结论

大多数用于这三个国家常见疾病的EMLc药物有支持证据,这与获批密切相关,而大量用于NIDs的药物在这三个国家未获批,无论它们是否有支持证据。由于高收入国家对EMLc的贡献有限,需要为制药公司建立适当的激励机制,以使针对NIDs的儿科药物研发可行且有效。

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