Tuesday, March 24, 2026
Phase 2 Data Support OCU410 in GA
After positive 12-month results from the ArMaDa trial, Ocugen plans a registrational phase 3 study of its investigational gene therapy.
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Ophthalmology Management
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Retinal Physician
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Glaucoma Physician
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Ophthalmic Professional
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The Ophthalmic ASC
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Presbyopia Physician
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Corneal Physician
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New Retinal Physician
Tuesday, March 24, 2026
After positive 12-month results from the ArMaDa trial, Ocugen plans a registrational phase 3 study of its investigational gene therapy.
Monday, March 23, 2026
A recent study finds the Multi-Luminance Shape Discrimination Test correlates with visual acuity, visual fields, and patient-reported outcomes.
Wednesday, March 18, 2026
Early data in treatment-naïve nAMD show visual gains and favorable pharmacokinetics.
Tuesday, March 10, 2026
Data from a phase 2a study in China suggest visual acuity gains and potential treatment durability.
Tuesday, March 3, 2026
During a symposium, investigators presented findings from the phase 3 SOL-1 trial highlighting the intravitreal insert’s durability and improved visual outcomes in patients with nAMD.
Monday, March 2, 2026
COMO and CAPRI will evaluate the intravitreal vorolanib insert vs the standard of care in treatment-naïve and previously treated patients with diabetic macular edema.
Monday, March 2, 2026
Early functional and anatomical gains observed at 3 months in the first adult patient treated with the subretinal gene therapy.
Thursday, February 19, 2026
As part of its ongoing ROP Education and Support Initiative, Prevent Blindness has declared the third annual Retinopathy of Prematurity (ROP) Awareness Week, Feb. 23 to March 1.
Wednesday, February 18, 2026
The deal adds ERG-focused retinal diagnostics to Ametek's portfolio.
Wednesday, February 11, 2026
The AI-driven 3D model maps polarity changes relevant to AMD progression, which could guide future therapeutic approaches.
Tuesday, February 10, 2026
The phase 3 4FRONT-1 study compares 4D-150, an investigational gene therapy, against aflibercept 2 mg in treatment-naïve patients.
Friday, February 6, 2026
The agreement grants MeiraGTx exclusive rights to ZipBio’s complement-targeting therapies for geographic atrophy.
Tuesday, February 3, 2026
The Aeye-DS device uses AI to allow non-ophthalmic providers to capture retinal images and screen for diabetic retinopathy.
Tuesday, February 3, 2026
Artevo 750 and 850 integrate digital and optical visualization for ophthalmic surgery.
Wednesday, January 28, 2026
The Abu Dhabi–based study will evaluate an investigational AAV therapy for MERTK-related retinitis pigmentosa.
Monday, January 26, 2026
NOV05, a topical tacrolimus ophthalmic solution, is set to enter a phase 2 trial in patients with noninfectious anterior uveitis.
Monday, January 26, 2026
The investigational cell therapy from Bayer AG/BlueRock Therapeutics is being studied for inherited photoreceptor diseases, including retinitis pigmentosa.
Thursday, January 22, 2026
The French company’s PST-611, which is being evaluated in a phase 1 trial, targets iron dysregulation in dry AMD and geographic atrophy.
Tuesday, January 20, 2026
Sakigake designation supports expedited review; FDA, EMA, and Japan conditionally approve the brand name Mogenry for Nanoscope’s optogenetic therapy.
Tuesday, January 20, 2026
Interim ArMaDa data show a reduction in lesion growth with no serious safety signals reported for Ocugen's investigational gene therapy.
Friday, January 16, 2026
The phase 1/2 trial is evaluating a dual-AAV gene therapy for Usher syndrome type 1B.
Tuesday, January 13, 2026
The companies will collaborate on home monitoring and connected care for chronic retinal disease.
Thursday, January 8, 2026
The next-generation VEGF/Ang2 bispecific antibody demonstrates rapid retinal drying and vision gains in patients with diabetic macular edema.
Thursday, January 8, 2026
Complement Therapeutics’s CTx001, an investigational gene therapy that targets complement pathways in geographic atrophy, will be evaluated in a phase 1/2 trial in 2026.
Wednesday, January 7, 2026
The patent extends US intellectual property protection for Nanoscope’s multicharacteristic opsin (MCO) platform through at least 2039.
Tuesday, January 6, 2026
The partnership with VectorBuilder aims to advance IKAR-003, an intravitreal gene therapy designed to slow AMD progression.
Tuesday, January 6, 2026
In a phase 2 trial, the drug showed functional and structural signals in optic neuritis.
Friday, January 2, 2026
Ranibizumab-leyk (Nufymco) is approved for for wet AMD, DME, DR, RVO-related macular edema, and myopic CNV.
Friday, January 2, 2026
The agency says Outlook Therapeutics must provide additional evidence confirming the efficacy of its intravitreal bevacizumab formulation for wet AMD.
Friday, January 2, 2026
Results underscore the potential of alternate objective measures in the pediatric population.