---
title: RYZUMVI FDA Approval for Presbyopia | Opus and Viatris
description: RYZUMVI gains FDA approval for presbyopia in adults. Explore how the eye drops work and the roles of Opus Genetics and Viatris.
image: https://visionexecutives.com/hubfs/AI-Generated%20Media/Images/Hand%20Holding%20Ryzumvi%20Eye%20Drops%20At%20Cafe.png
---

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# RYZUMVI FDA Approval for Presbyopia | Opus and Viatris

Oct 22, 2026, 4:40:42 PM

[Vision Executives](https://visionexecutives.com/blog/author/vision-executives)

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### RYZUMVI receives FDA approval for presbyopia in adults.

Reading a menu, checking a message or reviewing a document can become less comfortable as near vision changes with age. Presbyopia is a familiar part of that exercise, and a new FDA approval adds another prescription treatment option. 

Opus Genetics and Viatris announced FDA approval of RYZUMVI (phentolamine ophthalmic solution 0.75%) for presbyopia in adults. 

The decision expands the eye drops' existing US indication for reversing pharmacologically induced pupil dilation. 

### How do RYZUMVI eye drops work?

The preservative-free formulation reduces pupil size without engaging the ciliary muscle. It offers a pharmacological approach to improving near vision. 

Opus Genetics reported that both pivotal Phase III studies, VEGA-2 and VEGA-3, met their primary and all key secondary efficacy endpoints. 

Presbyopia typically becomes noticeable in the early to mid-40s and can cause blurred near vision and eye strain. 

### What are the roles of Opus Genetics and Viatris?

The companies have a licensing agreement covering the development of phentolamine ophthalmic solution 0.75%, with Viatris holding exclusive US commercialisation rights. 

Viatris stated that it was exploring a US partner to commercialise RYZUMVI for presbyopia. Approval and commercial rollout are therefore separate parts of the story. 

### What does the approval mean for patients and clinicians?

Another prescription option creates more scope for individual treatment discussions. The relevant questions are how it fits a person's visual needs, clinical circumstances and daily routine. 

Safety remains part of the conversation. Common ocular adverse reactions in presbyopia studies included eye redness (21%) and irritation at the application site (16%). 

The approval broadens the available approaches to presbyopia management. How the treatment is introduced and adopted will shape its place in everyday eye care. 

 

 

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