Lentechs Announces Preliminary Results in Milestone Clinical Trial

Clinical Trial Evaluated its Investigational Contact Lens for Patients with Presbyopia

Lentechs, a clinical-stage ophthalmic medical device company developing a new generation of soft, suspended contact lens, designed to transform the treatment paradigm for presbyopia, today announced key results in a milestone clinical trial evaluating its investigational contact lens for patients with presbyopia and presbyopia with astigmatism.

Presbyopia is a natural part of aging characterized by a gradual loss of the eyes’ ability to focus on objects up close and impacts 120 million people in the United States and 2 billion worldwide.1 Currently available multifocal contact lenses often force a visual compromise, leading most presbyopes to choose glasses over a preference for contact lenses.2

Building on its robust R&D program as it develops a new generation of soft contact lens, analysis from the 7-day visual acuity primary endpoint showed that patients wearing APIOC experienced improved distance vision vs their successful, habitual, multifocal contact lenses, or vision comparable to their habitual prescription glasses. Specifically, the analysis showed:

  • Patients reported clinically meaningful, statistically significant improvement in high-and low-contrast distance vision with APIOC over their habitual multifocal contact lenses, while maintaining vision up close and in-between
  • Patients reported comparable vision at distance, intermediate and near, with APIOC as with their habitual prescription glasses
  • Comfort was generally comparable to patients’ habitual multifocal contact lens

“These results provide tremendous evidence that APIOC helps solve the visual compromise caused by currently available multifocal contact lenses,” said President and Chief Executive Officer of Lentechs, Mr. Robin G. Sears. “Data show that only 10-15% of presbyopes currently wear contact lenses, yet 70% of glasses wearing presbyopes want to wear them2,3 —APIOC will be the contact lens that finally helps bridge that divide for patients and practitioners.”

Designed specifically with presbyopes in mind, APIOC™ is a patented, first-of-its-kind line of soft, suspended contact lens designed to deliver exceptional, glasses-like vision at all distances. APIOC is first and foremost designed to utilize the eye’s anatomy rather than conform to it. Unlike traditional contact lenses, APIOC is suspended behind the upper eyelid, allowing for free, translational (up and down) eye movement, behind the rotationally stable, centered contact lens. By allowing the eye to freely move behind the APIOC lens, wearers can access the specific prescription needed for each visual distance correction. “Dr. Melissa Bailey and I envisioned a novel, translating, soft contact lens that was easy to fit and reliable for patients with presbyopia. It’s very rewarding to see these results from our clinical study with real-world patients,” stated Chief Medical Officer of Lentechs, Dr. Joseph Barr.

Lentechs board member and former Global President, Vision Care for Bausch and Lomb and former Johnson & Johnson Vision executive, Peter Valenti added, “These data represent some of the most promising results I’ve ever seen for solving the vision challenges presbyopes face in their desire to wear contact lenses. APIOC is a game-changer for optometrists and patients and will help give presbyopes the vision they deserve from a contact lens.”


1 Review of Optometric Business. 2013. Presbyopia Expected to Impact Billions Worldwide. Retrieved from: https://www.reviewob.com/presbyopia-expected-to-impact-billions-worldwide-3/
2 Rueff & Bailey, Presbyopic and Non-Presbyopic Contact Lens Opinions and Vision Correction Preferences, 
Contact Lens & Anterior Eye, Volume 40, Issue 5, P323-328, October 01, 2017.
3 Data on file, Lentechs. APIOC Concept, Quantitative Market Research Study, June 2020.

SourceLentechs

Hot this week

Cartessa Aesthetics Partners with Classys to Bring EVERESSE to the U.S. Market

Classys, which is listed on the KOSDAQ, is one of South Korea's most distinguished aesthetic technology manufacturers, with devices distributed in 80+ markets globally. This partnership marks Classys's official entry into the American marketplace, with Cartessa Aesthetics as the exclusive distributor for EVERESSE, launched under the Volnewmer brand in current global markets.

Stryker Launches Next-Generation of SurgiCount+

Now integrated with Stryker's Triton technology, SurgiCount+ addresses two key challenges: retained surgical sponges and blood loss assessment. Integrating these previously separate digital solutions provides the added benefit of a more efficient, streamlined workflow for hospitals notes Stryker.

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”