← Back

Wire · opportunities

FDA Approves Phentolamine Eye Drop for Presbyopia in Adults

Published

19 October 2026

Topic

opportunities

◆ Sectors

Medtech

◆ Geography

United States

◆ Source

Read at pharmacytimes.com →

◆ Verified

Fusion42 · 19 October 2026 · Fusion42 review

The FDA has approved phentolamine ophthalmic solution 0.75% (Ryzumvi; Viatris) for treating presbyopia in adults as a once-nightly eye drop, following positive phase 3 VEGA-2 and VEGA-3 trials demonstrating improved near vision. The approval offers a new therapeutic option for age-related near vision loss with manageable side effects and specific storage and administration guidelines.

This Wire brief sits within Fusion42's coverage of Medtech, and 4 sources have reported it between 17 Oct 2026 and 19 Oct 2026.

◆ ◆ The Wire takeaway

Your ophthalmic product portfolio just faced new competition from a nightly eye drop that preserves distance vision while improving near focus. This shifts the presbyopia treatment market and may change patient preferences and prescribing patterns overnight.

◆ Coverage

4 sources · first reported 17 Oct 2026 · latest 19 Oct 2026

◆ Related on Wire

◆ Topics

Medtechpresbyopiaophthalmologyfda-approvalphentolamineeye-drop