# The cost of drug repurposing: parallel economic evaluation of mirtazapine for severe breathlessness in the multinational BETTER-B trial

**Authors:** Peter May, Charles Normand, Adejoke O. Oluyase, Samantha Smith, Sarah T. Brown, Matthew Maddocks, Massimo Costantini, Sabrina Bajwah, Kathrin Kahnert, Steffen T. Simon, Karen Ryan, David C. Currow, Miriam J. Johnson, Simon P. Hart, Małgorzata Krajnik, Silvia Tanzi, Charlotte E. Bolton, Piotr Janowiak, Elena Turola, Caroline J. Jolley, Hannah Mather, Geraldine Murden, Luca Ghirotto, Bobbie Farsides, Julia M. Brown, Irene J. Higginson

PMC · DOI: 10.1186/s12913-025-13605-9 · BMC Health Services Research · 2025-11-04

## TL;DR

A study evaluated whether using the antidepressant mirtazapine for severe breathlessness in lung disease patients is cost-effective, finding it reduces quality of life and increases costs.

## Contribution

The paper introduces a parallel economic evaluation of drug repurposing in a multinational clinical trial, emphasizing cost-effectiveness alongside clinical outcomes.

## Key findings

- Mirtazapine reduced quality-adjusted life years (QALYs) compared to placebo.
- Mirtazapine was associated with higher total healthcare costs.
- The likelihood of mirtazapine being cost-effective was less than 3% at standard willingness-to-pay thresholds.

## Abstract

Breathlessness is a prevalent, distressing symptom in advanced respiratory disease. Proven treatments are lacking. Mirtazapine, an antidepressant, is increasingly prescribed. The placebo-controlled BETTER-B trial did not find significant clinical benefit of mirtazapine for severe breathlessness, and patient experiences were mixed. Given mirtazapine’s low cost and wide availability, it is important to understand effects more broadly.

We conducted a parallel cost-effectiveness analysis of mirtazapine versus placebo. BETTER-B recruited 225 adults with chronic obstructive pulmonary disease and/or Interstitial Lung Diseases in seven countries between 2021 and 2023. We calculated quality-adjusted life years (QALYs) using EuroQoL EQ-5D-5 L and national value sets, and combined self-reported healthcare and informal care frequencies with unit costs. Primary trial endpoint was at day 56, with sensitivity analysis at day 180 (trial exit).

In primary analysis mirtazapine reduced QALYs (-0.006 (95% confidence interval (CI): -0.012 to -0.001)) and was associated with higher total costs (+€231 (95% CI: -218 to + 680)). For willingness-to-pay thresholds of €20,000-€40,000 per QALY, mirtazapine had a 1%-2% likelihood of being cost-effective. These findings were substantively unaffected by sensitivity analyses to timeframe, perspective, outcome measurement, and modelling strategy.

Repurposing mirtazapine to treat severe breathlessness negatively impacted patient outcomes while being associated with higher formal and informal costs, and should be discouraged. Off-label prescribing of repurposed medicines without robust evidence risks unnecessary strain on healthcare systems and families. Economic evaluation within testing of repurposed medicines is important. Parallel cost-effectiveness analyses can deliver high-value information even when the efficacy trial finds no effect.

The online version contains supplementary material available at 10.1186/s12913-025-13605-9.

## Linked entities

- **Chemicals:** mirtazapine (PubChem CID 4205)
- **Diseases:** chronic obstructive pulmonary disease (MONDO:0005002)

## Full-text entities

- **Diseases:** breathlessness (MESH:D004417)
- **Chemicals:** mirtazapine (MESH:D000078785)

## Full text

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## Figures

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## References

14 references — full list in the complete paper: https://tomesphere.com/paper/PMC12584416/full.md

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Source: https://tomesphere.com/paper/PMC12584416