Knez Lea, Jazbar Janja, Kos Mitja
University of Ljubljana, Faculty of Pharmacy, 1000 Ljubljana, Slovenia.
University Clinic Golnik, 4204 Golnik, Slovenia.
Oncologist. 2025 Jul 4;30(7). doi: 10.1093/oncolo/oyaf092.
Early access programs (EAPs) and medicine donation programs (MDPs) enable patients to have access to new medicines prior to regulatory approval or national reimbursement, respectively. The objective of this study was to evaluate the characteristics and timeliness of EAPs and MDPs in Slovenia.
Originator medicines approved by the EMA through a centralized procedure from 2010 to 2019 were included in the study. Data on the EAPs and MDPs were obtained from the Agency for Medicinal Products and Medical Devices of Slovenia.
The EMA approved 458 new indications for 324 medicines during the study period. In Slovenia, a total of 58 medicine indications (12.7%) became available before national reimbursement, including 35 (7.6%) by EAPs and 26 (5.7%) by MDPs (3 through both programs). Among these, 35 (60.3%) medicine indications were associated with oncology. EAPs facilitated access to medicines a median of 21.0 months before reimbursement (24.7 months for oncology medicines). Initiating EAPs at the time of the marketing authorization application could potentially improve the time of early access by an additional 5.5 months (5.2 months for oncology). MDPs enabled access to medicines 9.5 months prior to reimbursement (9.4 months for oncology), with potential further improvement by 7.9 months with the initiation of access at the time of marketing authorization (5.7 months for oncology).
Our findings highlight Slovenia's successful implementation of EAPs and MDPs, with oncology emerging as the predominant focal area. The potential exists for improvements in the scope, timeliness, and transparency of information on EAPs and MDPs accessible to patients in Slovenia.
早期准入计划(EAPs)和药品捐赠计划(MDPs)分别使患者能够在监管批准或国家报销之前获得新药。本研究的目的是评估斯洛文尼亚EAPs和MDPs的特征和及时性。
本研究纳入了2010年至2019年通过集中程序由欧洲药品管理局(EMA)批准的原创药物。EAPs和MDPs的数据来自斯洛文尼亚药品和医疗器械局。
在研究期间,EMA批准了324种药物的458个新适应症。在斯洛文尼亚,共有58个药品适应症(12.7%)在国家报销之前可用,其中35个(7.6%)通过EAPs,26个(5.7%)通过MDPs(3个通过两个计划)。其中,35个(60.3%)药品适应症与肿瘤学相关。EAPs使患者在报销前中位21.0个月能够获得药物(肿瘤学药物为24.7个月)。在上市授权申请时启动EAPs可能会使早期获得药物的时间再提前5.5个月(肿瘤学药物为5.2个月)。MDPs使患者在报销前提前9.5个月能够获得药物(肿瘤学药物为9.4个月),在上市授权时启动获取可能会进一步提前7.9个月(肿瘤学药物为5.7个月)。
我们的研究结果突出了斯洛文尼亚在EAPs和MDPs方面的成功实施,肿瘤学成为主要重点领域。斯洛文尼亚患者可获取的EAPs和MDPs信息在范围、及时性和透明度方面仍有改进空间。