School of Pharmacy, Sungkyunkwan University, 2066 Seobu-ro, Jangan-gu, Suwon, Gyeong gi-do, 16419, South Korea.
Ther Innov Regul Sci. 2020 Mar;54(2):418-423. doi: 10.1007/s43441-019-00071-9. Epub 2020 Jan 6.
Although great efforts have been made to address delays in new-drug approvals between different regions, little is known regarding drug lag in Korea. We compared drug lag in Korea with that in Japan, which is well known through many previous studies.
We extracted approval information from public data obtained from the regulatory authorities on all new drugs that were listed in both Korea and Japan between 2009 and 2017. Relative drug lag represented the difference between the date of approval in the country of interest and the date of the first global approval. Relative drug lag was measured as median approval lag. Multiple regression models were used to identify the factors associated with drug lag. The factors considered included origin of substance, nationality of manufacturer, original approval date, orphan drug status, and therapeutic class.
In total, 394 new drugs were approved in both countries between 2009 and 2017. The median approval lag was 28.2 and 54.1 months in Korea and Japan, respectively. Domestic company drugs were associated with longer median approval lag in Korea ([Formula: see text]), sensory organ drugs were associated with shorter median approval lag in Japan ([Formula: see text]), and orphan drug status was associated with longer duration of drug approval in Japan ([Formula: see text]).
Notable drug lags were observed in both Korea and Japan, but the lag was shorter in Korea. Inclusion of global clinical trials and existence of prior knowledge in new drug development were critical to reduce drug lag.
尽管在解决不同地区新药批准的延迟方面已经做出了巨大努力,但对于韩国的药物滞后问题却知之甚少。我们将韩国的药物滞后情况与日本进行了比较,日本在之前的许多研究中已经有了广泛的了解。
我们从监管机构公布的公共数据中提取了 2009 年至 2017 年间在韩国和日本上市的所有新药的批准信息。相对药物滞后表示感兴趣国家的批准日期与全球首次批准日期之间的差异。相对药物滞后以中位数批准滞后来衡量。使用多元回归模型来确定与药物滞后相关的因素。考虑的因素包括物质来源、制造商国籍、原始批准日期、孤儿药状态和治疗类别。
2009 年至 2017 年期间,两国共有 394 种新药获得批准。韩国和日本的中位批准滞后时间分别为 28.2 个月和 54.1 个月。在韩国,国内公司的药物与中位批准滞后时间较长相关([公式:见文本]),在日本,感觉器官药物与中位批准滞后时间较短相关([公式:见文本]),孤儿药状态与日本药物批准时间较长相关([公式:见文本])。
韩国和日本都存在显著的药物滞后现象,但韩国的滞后时间较短。纳入全球临床试验和新药开发中存在的先验知识对于减少药物滞后至关重要。