# Mirabegron in patients with age-related macular degeneration treated for overactive bladder: a study protocol for a prospective observational non-randomized trial

**Authors:** Lucia Ambrosio, Maurizio Cammalleri, Serena Panariello, Gianluigi Califano, Arianna Scala, Giovanni Improta, Antonio Pisani, Robert Rejdak, Ireneusz Ostrowski, Luca Filippi, Paola Bagnoli, Massimo Dal Monte, Mario Damiano Toro

PMC · DOI: 10.3389/fmed.2026.1761473 · 2026-03-16

## TL;DR

This study explores whether mirabegron, a drug for overactive bladder, might help prevent dry AMD from progressing to a more severe form.

## Contribution

The study introduces mirabegron as a potential therapy for slowing AMD progression in patients with overactive bladder.

## Key findings

- Mirabegron may influence retinal angiogenic proliferation, potentially reducing AMD conversion risk.
- The drug's safety profile in the eye supports its investigation for AMD treatment.
- The study aims to evaluate mirabegron's impact on AMD progression in patients with overactive bladder.

## Abstract

Although anti-vascular endothelial growth factor drugs have revolutionized the treatment of neovascular age-related macular degeneration (wet AMD), preventing eyes from converting from dry to wet AMD provides better long-term prognosis for sight and overall health. Mirabegron, an agonist at beta 3 adrenoceptors (β3-ARs), is licensed for the treatment of overactive bladder (OAB), but has potential effects on angiogenic proliferation in the retina, and therefore may reduce risk of conversion from dry to wet AMD. Both OAB and AMD are more common in older adults and share risk factors suggesting a potential link between these two conditions, thus highlighting the need for common therapy for the two diseases. Mirabegron use in AMD patients is supported by its rather safe profile at the eye level as macular and choriocapillary parameters do not seem to be affected in OAB patients. The purpose of this study will be to investigate the effects of mirabegron in patients concomitantly affected by OAB and dry AMD to evaluate its impact on slowing down AMD progression from the dry to the neovascular form.

https://clinicaltrials.gov/study/NCT07305298, identifier NCT07305298.

## Linked entities

- **Chemicals:** Mirabegron (PubChem CID 9865528)
- **Diseases:** age-related macular degeneration (MONDO:0005150), overactive bladder (MONDO:0006624)

## Full-text entities

- **Genes:** VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}
- **Diseases:** OAB (MESH:D053201), age-related macular degeneration (MESH:D008268), AMD (MESH:D006009), dry (MESH:D015352)
- **Chemicals:** Mirabegron (MESH:C520025)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13033596/full.md

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Source: https://tomesphere.com/paper/PMC13033596