# Cost-utility analysis of eptinezumab for migraine prevention in Taiwan

**Authors:** Cheng-Shen Chan, Tzu-Yao Huang, Wei-Hsuan Tseng, Tsung-Kun Lin, Fu-Chi Yang, Yi Liu, Yuan-Zhen Ruan, Ping-Hsuan Hsieh

PMC · DOI: 10.1186/s13561-025-00711-x · 2025-12-28

## TL;DR

This study evaluates whether eptinezumab, a migraine treatment, is cost-effective in Taiwan compared to a placebo.

## Contribution

This is the first study to assess the cost-effectiveness of eptinezumab for migraine prevention in Taiwan.

## Key findings

- Eptinezumab had an ICER of $73,929 per QALY gained, which is below the exploratory threshold of three times GDP per capita.
- Utility values for migraine frequency were the most influential factor in the cost-effectiveness model.
- Eptinezumab was found to be cost-effective in 98% of probabilistic sensitivity analysis iterations at the higher threshold.

## Abstract

Migraine is a neurological disorder prevalent in Taiwan, affecting millions of individuals and imposing a substantial burden on both quality of life and societal productivity. Calcitonin gene-related peptide inhibitors, such as eptinezumab, represent a major advancement in migraine prevention; however, their high cost and the lack of local economic evaluations warrant further study. This research aims to assess the cost-effectiveness of eptinezumab, compared with placebo, for migraine prevention in Taiwan.

A Markov model with a six-month time horizon was developed to evaluate the cost-effectiveness of eptinezumab versus placebo. The analysis was conducted from a health payer’s perspective, incorporating clinical and economic inputs from clinical trials and the literature. Patients were categorized into six health states based on monthly migraine days. Outcomes were expressed as incremental costs per quality-adjusted life year (QALY) gained. Incremental cost-effectiveness ratios (ICERs) were estimated using a Monte Carlo simulation with 10,000 iterations, alongside deterministic and probabilistic sensitivity analyses to evaluate uncertainty. For interpretation, results were compared with Taiwan’s GDP per capita ($32,327 per QALY), and exploratory analyses also considered a threshold of three times GDP per capita ($96,981).

Over six months, the total cost for patients receiving eptinezumab was $4,461, compared with $1,065 for placebo, with corresponding QALYs of 0.35 and 0.31, respectively. This yielded an ICER of $73,929 per QALY gained. Deterministic sensitivity analysis identified utility values for patients with varying migraine frequency as the most influential parameter, increasing the ICER to approximately $105,000 when varied, which may exceed the upper WTP threshold. Probabilistic sensitivity analysis showed that eptinezumab was cost-effective in 98% of iterations at the exploratory threshold of three times GDP per capita.

Eptinezumab was likely cost-effective for migraine prevention in Taiwan, with utility values associated with migraine frequency identified as the key driver, highlighting the need for locally relevant quality-of-life data in future evaluations.

The online version contains supplementary material available at 10.1186/s13561-025-00711-x.

• This study is the first to evaluate the cost-effectiveness of eptinezumab for migraine prevention in Taiwan.

• Eptinezumab demonstrated an incremental cost-effectiveness ratio of $73,929 per QALY gained and is considered cost-effective in the context.

• Utility values associated with different levels of migraine frequency were the most influential factor affecting the model outcomes.

The online version contains supplementary material available at 10.1186/s13561-025-00711-x.

## Linked entities

- **Diseases:** migraine (MONDO:0005277)

## Full-text entities

- **Diseases:** neurological disorder (MESH:D009461), Migraine (MESH:D008881)
- **Chemicals:** Eptinezumab (MESH:C000628361)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12860139/full.md

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Source: https://tomesphere.com/paper/PMC12860139