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斯洛文尼亚药品早期准入计划及捐赠的特点与可得性

Characteristics and availability of medicine early access programs and donations in Slovenia.

作者信息

Knez Lea, Jazbar Janja, Kos Mitja

机构信息

University of Ljubljana, Faculty of Pharmacy, 1000 Ljubljana, Slovenia.

University Clinic Golnik, 4204 Golnik, Slovenia.

出版信息

Oncologist. 2025 Jul 4;30(7). doi: 10.1093/oncolo/oyaf092.

DOI:10.1093/oncolo/oyaf092
PMID:40694381
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12282359/
Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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).

CONCLUSION

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.

摘要

背景

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。

方法

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。

结果

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)。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47f4/12282359/948f69f40ba7/oyaf092_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47f4/12282359/9b6814373f21/oyaf092_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47f4/12282359/948f69f40ba7/oyaf092_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47f4/12282359/9b6814373f21/oyaf092_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47f4/12282359/948f69f40ba7/oyaf092_fig2.jpg

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ESMO Open. 2023 Aug;8(4):101593. doi: 10.1016/j.esmoop.2023.101593. Epub 2023 Jul 4.
2
Early access provision: Awareness, educational needs and opportunities to improve oncology patients' access to care.早期准入规定:提高肿瘤患者就医机会的认知、教育需求及机遇
Front Oncol. 2022 Oct 26;12:714516. doi: 10.3389/fonc.2022.714516. eCollection 2022.
3
International Country-Level Trends, Factors, and Disparities in Compassionate Use Access to Unlicensed Products for Patients With Serious Medical Conditions.
国际层面严重疾病患者未获许可产品同情使用准入的趋势、影响因素和差异。
JAMA Health Forum. 2022 Apr 15;3(4):e220475. doi: 10.1001/jamahealthforum.2022.0475. eCollection 2022 Apr.
4
Sustainable medicines use in clinical practice: A clinical pharmacological view on eco-pharmaco-stewardship.临床实践中的可持续药物使用:生态药物管理的临床药理学观点。
Br J Clin Pharmacol. 2022 Jul;88(7):3023-3029. doi: 10.1111/bcp.15140. Epub 2021 Dec 6.
5
Comparative study on anticancer drug access times between FDA, EMA and the French temporary authorisation for use program over 13 years.13年间美国食品药品监督管理局、欧洲药品管理局及法国临时使用授权程序的抗癌药物获取时间对比研究
Eur J Cancer. 2021 May;149:82-90. doi: 10.1016/j.ejca.2021.03.008. Epub 2021 Apr 7.
6
Access to innovation through the national early access program and clinical trials for patients with malignant melanoma.通过国家早期准入计划和临床试验为恶性黑色素瘤患者获取创新药物。
Cancer. 2021 Jul 1;127(13):2262-2270. doi: 10.1002/cncr.33492. Epub 2021 Mar 25.
7
Early Access Provision for Innovative Medicinal Products in Oncology: Challenges and Opportunities.肿瘤学创新药物的早期准入规定:挑战与机遇
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8
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Achieving equal and timely access to innovative anticancer drugs in the European Union (EU): summary of a multidisciplinary CECOG-driven roundtable discussion with a focus on Eastern and South-Eastern EU countries.实现欧盟成员国平等、及时地获得创新抗癌药物的机会:以中东欧和东南欧国家为重点的跨学科 CECOG 驱动圆桌讨论综述。
ESMO Open. 2019 Nov 13;4(6):e000550. doi: 10.1136/esmoopen-2019-000550. eCollection 2019.
10
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JAMA Netw Open. 2018 Jun 1;1(2):e180283. doi: 10.1001/jamanetworkopen.2018.0283.