September 17th 2025
In addition to the proxy statement, STAAR has reached out to all stockholders to ask for their vote to adopt the merger agreement.
September 17th 2025
Geographic atrophy survey reveals heavy emotional burden, decreased independence for patients
April 26th 2022Apellis Pharmaceuticals releases results of their Geographic Atrophy Insights Survey (GAINS), revealing a large emotional toll and significant decrease in independence for patients with geographic atrophy.
Digital health care in ophthalmology: Opportunities and limitations for retina specialists
April 25th 2022Over the past 2 years, retina specialists and their patients have learned how AI may be a tool physicians can use to monitor patients for disease progression, how telemedicine might mean more than a mere video chat between patient and clinician, and how the tools of the 21st century were closer to real-world practice than anticipated.
Diving into the relationship between amblyopia and fixation eye movements
April 23rd 2022In patients with amblyopia, minuscule fixation eye movements play a major role with treatment, according to Fatema Ghasia, MD, associate professor of ophthalmology and director of the Vision Neuroscience and Ocular Motility Laboratory at the Cole Eye Institute at Cleveland Clinic in Ohio.
Illuminate trial updates: Additional analyses required for sepofarsen for LCA10
April 16th 2022According to the company, post-hoc analyses from Illuminate trial of sepofarsen demonstrate an encouraging efficacy signal when comparing active treatment and sham eyes to their corresponding contralateral eyes across multiple endpoints. The company plans to discuss findings with regulators in Q3.
First pediatric patient dosed in LCA10 gene editing clinical trial
April 13th 2022The trial marks the first-ever in vivo delivery of an experimental CRISPR gene editing medicine to a pediatric patient, with the company on track to complete dosing of the pediatric mid-dose cohort in the first half of 2022.
UCI study cites base editing as a durable one-time treatment for inherited retinal degeneration
April 12th 2022According to researchers at the University of California, Irvine, base editing may provide long-lasting retinal protection and prevent vision deterioration in patients with inherited retinal degeneration, specifically in Leber congenital amaurosis patients.
Trial to study treatment of DME in underrepresented patients begins
April 11th 2022The trial will study the effect of the drug in treatment-naïve patients with diabetic macular edema (DME) who are members of underrepresented patient populations, ie, Black, Hispanic, Latin American, and Indigenous people.
"Focus on Child Eye Health" presented by International Agency for the Prevention of Blindness
April 10th 2022The International Agency for the Prevention of Blindness (IAPB) recently announced an expansion of their ‘Focus on Glaucoma’ and ‘Focus on Diabetes’ series with their new ‘Focus on Child Eye Health’ series in partnership with CooperVision.
Outcomes of anti-VEGF therapy for retinal diseases altered by COVID-19 lockdown
April 8th 2022Investigators found that patients with neovascular age-related macular degeneration in all countries included in the study lost vision as a result of the lockdown and reduced number of treatments during the COVID-19 pandemic.
Gene required for survival of retinal ganglion cells identified by Japanese investigators
April 5th 2022A team of investigators at the Okinawa Institute of Science and Technology Graduate University in Japan have identified a gene necessary for the survival of retinal ganglion cells—a class of neurons located in the retina that are critical for vision.
UPLIZNA safe, effective for patients with neuromyelitis optica spectrum disorder
April 2nd 2022Horizon Therapeutics announces new data and a separate analysis will be presented at the American Academy of Neurology 2022 Annual Meeting, showing that UPLIZNA reduced disease activity associated with neuromyelitis optica spectrum disorder (NMOSD) over 3 years.
Outlook Therapeutics submits BLA for ophthalmic bevacizumab ONS-5010 as treatment for wet AMD
March 31st 2022If the Biologics License Application is approved by the FDA, the company could receive 12 years of marketing exclusivity for an FDA-approved alternative for the most frequently used anti-VEGF treatment in wet AMD patients in the United States.