Healthcare Group, Lee&Ko , Seoul, Republic of Korea.
Department of Market Access, AbbVie Korea , Seoul, Republic of Korea.
Expert Rev Pharmacoecon Outcomes Res. 2021 Feb;21(1):119-126. doi: 10.1080/14737167.2020.1758559. Epub 2020 Apr 26.
: This study aims to provide an up-to-date analysis of the current state of patient access to new drugs in South Korea, focusing on the effect of new review pathways for reimbursement. : We analyzed patients' access to new drugs, listing rate and lead time until listing from marketing authorization. New pathways were defined as 'price negotiation waiver,' 'risk-sharing agreements,' and 'pharmacoeconomic evaluation exemption.' : The listing rate for drugs increased after the introduction of the new pathways (93.7% vs. 77.9%, p < 0.001). Before the new pathways, the median lead time for listing was 21.0 months (95% CI: 16.9-25.0), while afterward it was shortened to 10.9 months (95% CI: 10.2-11.7) (p < 0.001). : Although it has strengthened national health insurance coverage by positively impacting the rate and lead time, the lead time for the oncology and orphan drugs is substantially longer as compared to other drugs. Expanding the eligibility criteria to include non-life-threatening but rare or intractable diseases, and resolving the system's operational issues are still necessary.
这项研究旨在对韩国新药患者可及性的现状进行最新分析,重点关注新的报销审查途径的影响。
我们分析了新药的患者可及性、上市率和从获得上市许可到上市的时间。新途径被定义为“免除价格谈判”、“风险分担协议”和“药物经济学评价豁免”。新途径引入后,药品上市率提高(93.7%对 77.9%,p<0.001)。在新途径之前,上市的中位时间为 21.0 个月(95%CI:16.9-25.0),之后缩短至 10.9 个月(95%CI:10.2-11.7)(p<0.001)。
虽然通过积极影响上市率和上市时间来加强国家健康保险覆盖范围,但与其他药物相比,肿瘤药物和孤儿药物的上市时间要长得多。扩大资格标准,将非危及生命但罕见或难治性疾病包括在内,并解决系统的操作问题仍然是必要的。