
Articles
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1 day ago |
optometrytimes.com | AnnMarie Hipsley |Emily Kaiser Maharjan |Sheryl Stevenson |Hattie Hayes
At the 2025 ASCRS meeting in Los Angeles, a concept was shared by AnnMarie Hipsley, DPT, PhD, for optometrists seeking to stay at the forefront of precision ocular care—the Digital Twin. More than a buzzword, a digital twin represents a virtual simulation of a real-world anatomical system, in this case, the human eye.
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5 days ago |
optometrytimes.com | Mark Bullimore |Martin Harp |Hattie Hayes |Emily Kaiser Maharjan
At the 2025 ARVO conference in Salt Lake City, Mark Bullimore, MCOptom, PhD, of the University of Houston College of Optometry shared a compelling critique of the current use of centile growth curves for axial length in myopia management. Speaking directly to optometrists, Bullimore emphasized the need for more accurate, condition-specific tools in evaluating myopic eye growth and treatment efficacy. Centile growth curves based on general populations are misleading in myopia management.
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6 days ago |
optometrytimes.com | Emily Kaiser Maharjan
Cognition Therapeutics reported topline results for the phase 2 Magnify trial of the oral medication zervimesine intended to slow lesion growth in patients with geographic atrophy (GA) secondary to dry age-related macular degeneration (dry AMD). At 18 months, patients who were treated with zervimesine had 28.6% slower GA lesion growth and their lesions were 28.2% smaller than patients in the placebo growth.
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6 days ago |
optometrytimes.com | Emily Kaiser Maharjan
Boehringer Ingelheim announced the start of the JADE and VERDANT phase 2 clinical studies to investigate the safety and efficacy of 2 candidates: BI 1584862, a potential first-in-class oral compound for the treatment of geographic atrophy (GA), an advanced form of age-related macular degeneration (AMD)1; and BI 771716, an antibody fragment, respectively. BI 1584862 is a phospholipid modulator intended to preserve patient vision by targeting inflammation and preserving vascular function.
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6 days ago |
optometrytimes.com | Emily Kaiser Maharjan
Today, Luminopia announced that its amblyopia treatment has been approved by Anthem Blue Cross and Blue Shield for insurance coverage.1 The news comes on the heels of the FDA’s age extension of clearance for Luminopia’s amblyopia treatment, now indicating treatment from patients aged 4 to 7 to patients aged 4 to 12 years.2 Both are steps toward expanding access to the unique, entertainment-based amblyopia treatment nationwide.
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