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경제성평가자료제출생략 트랙으로 진입한 약제에 대한 외국의 치료적 이익 평가 결과 비교Comparative Review of Added Health Benefits of the Drugs Listed through Economic Evaluation Exemption Procedure in Korea: Cases of France, Germany, and Canada

Other Titles
Comparative Review of Added Health Benefits of the Drugs Listed through Economic Evaluation Exemption Procedure in Korea: Cases of France, Germany, and Canada
Authors
배은영차소희임화령이혜재홍지형
Issue Date
Feb-2024
Publisher
대한약학회
Keywords
Economic Evaluation Exemption Procedure; Additional benefit; Comparative analysis; Therapeutic value; Health technology assessment
Citation
약 학 회 지, v.68, no.1, pp 62 - 70
Pages
9
Indexed
KCI
Journal Title
약 학 회 지
Volume
68
Number
1
Start Page
62
End Page
70
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/71280
DOI
10.17480/psk.2024.68.1.62
ISSN
0377-9556
2383-9457
Abstract
This study assessed the additional health benefits of the drugs listed through the Economic EvaluationExemption Procedure (EEEP) in Korea. We conducted a comparative review of 32 EEEP drugs listed between May 2015and July 2022, comparing how they were assessed in France, Germany, and Canada. To collect the data, we reviewed theevaluations conducted by the relevant agency in each country and identified if the additional benefit exists and howsignificant it is. Additionally, the size of the benefit gains assessed by each agency was categorized as "High" or "Low,"allowing us to evaluate the consistency among these countries. In France, only 38% of the 34 drugs compareddemonstrated moderate or higher levels of additional benefit. Germany acknowledged substantial benefit improvement in27% of the 30 drugs assessed, while 73% showed minor, unquantifiable, or no additional benefits. In Canada, 5 out of22 cases have been identified as providing significant additional benefit. The level of inter-country consistency in theassessment results from these three countries was somewhat limited. Based on the evaluation results in France, Germany,and Canada, the additional benefits of EEEP drugs over existing treatments were not substantial in many cases. Eventhough the EEEP was introduced to improve accessibility to high-cost drugs for medical conditions with unmet needs, itis necessary to reconsider whether to allow exceptions for drugs with low therapeutic value.
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