Hyewon Jeon, Sang-In Park, Sang-Won Lee, Tae-Eun Kim, Kwang-Hee Shin, Ildae Song, Hyewon Chung, Byoungjun Bae, Sonu Baik, Namyi Gu
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引用次数: 0
Abstract
In recent years, with the experience of the COVID-19 pandemic, countries around the world have realized that improving patient access to new medicines can have a significant impact on public health and economic stability. The aim of this study was to identify new drugs that are urgently needed among those not yet available in South Korea from 2011 to 2020, and to develop strategies to improve access by analyzing the causes of delay. Through a 3-step screening process that included a literature review of new drugs, surveys of domestic clinicians and academics, and consideration of expedited review status by regulatory authorities, 34 out of 244 unreleased new drugs were prioritized for rapid introduction. Reasons for drug delays were investigated through inquiries to the marketing authorization holders of the prioritized drugs and interviews with experts on new drug introductions. Key considerations for market entry include exemption from bridging clinical trials, reimbursement listing, and maximum reimbursement price. For foreign developers without domestic subsidiaries, providing systematic support-such as clear information on Korea's regulatory standards and facilitating reliable partnership matching-could improve access to priority unintroduced new drugs. Based on the results of this study, we propose strategies to facilitate the introduction of priority new drugs in South Korea.
期刊介绍:
Translational and Clinical Pharmacology (Transl Clin Pharmacol, TCP) is the official journal of the Korean Society for Clinical Pharmacology and Therapeutics (KSCPT). TCP is an interdisciplinary journal devoted to the dissemination of knowledge relating to all aspects of translational and clinical pharmacology. The categories for publication include pharmacokinetics (PK) and drug disposition, drug metabolism, pharmacodynamics (PD), clinical trials and design issues, pharmacogenomics and pharmacogenetics, pharmacometrics, pharmacoepidemiology, pharmacovigilence, and human pharmacology. Studies involving animal models, pharmacological characterization, and clinical trials are appropriate for consideration.