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Lenz Therapeutics Receives FDA Approval of VIZZ for the Treatment of Presbyopia

07/31/2025
Lenz Therapeutics Receives FDA Approval of VIZZ for the Treatment of Presbyopia image

A new, first-of-its kind presbyopia drop will soon be available in the US as the FDA approved Lenz Therapeutics' VIZZ (aceclidine ophthalmic solution) 1.44%. Expected to be broadly available in the fourth quarter of 2025, VIZZ is the first and only FDA-approved aceclidine-based eye drop for the treatment of presbyopia in adults.

“We believe yesterday's approval will establish a new standard-of-care in presbyopia. As we have shown, this is not only best-in-class, but frankly, the only in a class of pupil selective ciliary-sparing myotics," Eef Schimmelpennink, President and Chief Executive Officer of Lenz Therapeutics, said in investor call on Friday. “This is uniquely engineered, highly-differentiated and designed to deliver quick onset and lasting benefit for the vast majority of presbyopes."

According to Lenz, VIZZ has a differentiated mechanism of action as a predominantly pupil-selective miotic that interacts with the iris, with minimal ciliary muscle stimulation. VIZZ contracts the iris sphincter muscle resulting in a pinhole effect and uniquely achieves a sub-2mm pupil that extends depth of focus to significantly improve near vision without causing a myopic shift. Aceclidine, the sole active ingredient in VIZZ, is a new chemical entity in the United States and its FDA approval marks a global first in the treatment of presbyopia. Mr. Schimmelpennink said VIZZ is the first and only once-daily eye drop with proven efficacy for up to 10 hours into the market.

"Because we don't stimulate the ciliary body, we're actually able to have a product that gets you to below 2 millimeters. If you do that with any other meiotic and you move somebody to below 2 millimeters, you're dramatically impacting negatively that distance vision. But also that stimulation of the ciliary body really puts a lot of tension on the retina, which obviously something that you want to avoid," Mr. Schimmelpennink said in an interview with Eyewire+.

The FDA approval of VIZZ was based upon results from three randomized, double-masked, controlled phase 3 studies. CLARITY 1 and CLARITY 2 were designed to evaluate the safety and efficacy of VIZZ in 466 participants dosed once daily for 42 days. CLARITY 3 evaluated 217 participants for long term safety over a 6-month duration of once daily dosing.

In both CLARITY 1 and CLARITY 2, VIZZ achieved all primary and secondary near vision improvement endpoints, demonstrating the ability to improve near vision within 30 minutes and last up to 10 hours. Near vision improvement was reproducible and consistent across both CLARITY 1 and 2. VIZZ was well-tolerated with no serious treatment-related adverse events observed in the over 30,000 treatment days across all three CLARITY trials. The most common reported adverse reactions of participants were installation site irritation, dim vision and headache. The majority of adverse reactions were mild, transient and self-resolving.

“This FDA approval represents a disruptive paradigm shift in treatment options for millions of people who are frustrated and struggling with the inevitable age-related loss of their near vision,” said VIZZ clinical investigator Marc Bloomenstein, OD, FAAO, of Schwartz Laser Eye Care Center in Scottsdale, Arizona. “I believe this will be a welcome solution for both optometrists and ophthalmologists who will now be able to offer a highly effective and sought-after presbyopia treatment that could immediately become the standard of care, with a product profile that will meet our patients’ needs.”

During the investor call, Lenz executives outlined the cost of VIZZ. A monthly, 25-pack will cost $79. A 3-month pack from the e-pharmacy will cost $198 ($66 per month). Samples are anticipated in the United States as early as October 2025, with commercial product to be broadly available by mid-Q4 2025. Direct-to-eye care professional sales and marketing activities to be initiated immediately, according to Lenz.

For more information about VIZZ and full prescribing information, visit www.VIZZ.com.

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