Department of Clinical Medicine (Pharmaceutical Medicine), Graduate School of Pharmaceutical Sciences, Kitasato University, 5-9-1 Shirokane, Minato-Ku, Tokyo, 108-8641, Japan.
Ther Innov Regul Sci. 2023 Jul;57(4):671-677. doi: 10.1007/s43441-023-00512-6. Epub 2023 Mar 25.
Drug lag in Japan has greatly decreased over the past decades; however, new instances of drug lag have appeared along with changes in the circumstances of oncology drug development. We aimed to investigate the factors associated with the approval lag for new oncology drugs between Japan and the United States (US) over the past decade by comparing approval dates and modalities, lead indications, approval types, and phase I strategies for earlier approval in Japan.
We descriptively evaluated the characteristics of 117 new oncology drugs approved in either Japan or the US from January 1, 2011, to December 31, 2020.
Seventy-one drugs were approved in Japan, 112 in the US, five only in Japan, and 46 only in the US. Interestingly, new oncology drugs were predominantly developed by the top 20 pharmaceutical companies in Japan; however, the opposite was true for drugs that were not yet approved in Japan. However, no clear trend was observed in the relationship between drug lag and the studied factors, except for the phase I strategy. There was a numerical but clear trend in which a higher percentage of phase I multiregional clinical trials (MRCTs) in the drug development strategy was observed for drugs with earlier approval in Japan.
Participation in global drug development during the early stages, such as during phase I MRCTs, is one of the keys to successfully minimizing this new instance of drug lag in Japan.
在过去几十年中,日本的药品滞后现象已经大大减少;然而,随着肿瘤药物开发环境的变化,新的药品滞后现象也出现了。我们旨在通过比较日本早期批准的新药的批准日期和模式、主要适应证、批准类型和 I 期策略,调查过去十年中日美新肿瘤药物批准延迟的相关因素。
我们描述性地评估了 2011 年 1 月 1 日至 2020 年 12 月 31 日期间在日本或美国批准的 117 种新肿瘤药物的特征。
71 种药物在日本获得批准,112 种在美国获得批准,5 种仅在日本获得批准,46 种仅在美国获得批准。有趣的是,新的肿瘤药物主要由日本前 20 大制药公司开发;然而,对于尚未在日本获得批准的药物则相反。然而,除了 I 期策略外,没有明显的趋势表明药物滞后与所研究的因素之间存在关系。在药物开发策略中,I 期多区域临床试验(MRCT)的比例越高,日本批准的药物就越早,这一趋势虽然是数字上的,但却很明显。
在早期阶段参与全球药物开发,如 I 期 MRCT,是成功减少日本这种新的药品滞后现象的关键之一。