Cost–effectiveness analysis of prolonged-release fampridine to treat walking disability of multiple sclerosis in China

Author:

Zhao Xinran1ORCID,Yang Han1,Wei Tian1,Zhao Jin1,Liu Jun1,Huang Zhe2,Zhu Lin2,Zhao Yinan3ORCID,Li Wei4ORCID

Affiliation:

1. Real World Solutions, IQVIA, Shanghai, 200124, China

2. Value & Access, Biogen China, Shanghai, 200031, China

3. The First Hospital of China Medical University, Shenyang, Liaoning, 110001, China

4. School of International Pharmaceutical Business, China Pharmaceutical University, Nanjing, Jiangsu, 211198, China

Abstract

Objectives: This study evaluates the cost–effectiveness of adding prolonged-release (PR)-fampridine to best supportive care (BSC) versus BSC alone in adult multiple sclerosis patients with walking disability in China. Materials & methods: A hybrid decision tree and Markov model from both the societal and healthcare perspectives were constructed. Parameters were derived from clinical trials of PR-fampridine, published sources and clinical expert interviews. Results: Over a 10-year time horizon, adding PR-fampridine to BSC led to 0.15 quality-adjusted life year (QALY) gain and lower costs, with incremental cost–effectiveness ratios of -238,806 Chinese Yuan/QALY and -113,488 Chinese Yuan/QALY from the societal and healthcare perspectives, respectively. Conclusion: Compared with BSC alone, PR-fampridine plus BSC is considered an economically dominant strategy for the treatment of multiple sclerosis-related walking disability in China.

Funder

Biogen

Publisher

Becaris Publishing Limited

Subject

Health Policy

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