Make a table for recent advances in glaucoma treatment
glaucoma treatment advances
recent advances glaucoma treatment 2024 2025 new therapies
glaucoma minimally invasive surgery MIGS outcomes
https://www.reviewofophthalmology.com/article/the-2026-glauc…
PMID: 37742700
glaucoma neuroprotection gene therapy clinical trial
| Category | Advance | Details / Examples | Status (2025-2026) | Key Evidence |
|---|---|---|---|---|
| Novel Pharmacology - Rho Kinase (ROCK) Inhibitors | Netarsudil (Rhopressa) | Lowers IOP by increasing trabecular meshwork outflow and reducing episcleral venous pressure; also reduces aqueous production. Fixed-dose combo with latanoprost (Rocklatan) available. | FDA-approved; in clinical use | Kanski's Clinical Ophthalmology 10th ed.; PMC12460366 |
| Novel Pharmacology - Nitric Oxide Donors | Latanoprostene bunod (Vyzulta) | Releases nitric oxide to relax the trabecular meshwork via cGMP pathway, enhancing conventional outflow alongside uveoscleral outflow. Dual mechanism of action. | FDA-approved; in clinical use | Katzung's Basic & Clinical Pharmacology 16th ed.; PMC12460366 |
| Sustained-Release Drug Delivery | iDose TR (travoprost implant) | Biocompatible titanium intracameral implant providing 24/7 sustained travoprost release. FDA approved December 2023 based on two Phase 3 pivotal trials (n=1,150) meeting all primary endpoints. Eliminates drop compliance issues. | FDA-approved (Dec 2023) | PMC12460366 |
| Sustained-Release Drug Delivery | Bimatoprost SR (Durysta) | Biodegradable intracameral implant releasing bimatoprost; single injection sustained effect for months. | FDA-approved | PMC12460366 |
| Sustained-Release Drug Delivery | ENV515 / Travoprost XR (Envisia Therapeutics) | Phase 2 data shows 11-month duration-of-action after a single intravitreal dose in glaucoma patients. | Phase 2 (active) | 2026 Glaucoma Pipeline |
| Sustained-Release Drug Delivery | PolyActiva ocular micro-implant | Drug-eluting subconjunctival polymer micro-implant; Phase 2b US trial active (first patient enrolled). | Phase 2b | 2026 Glaucoma Pipeline |
| Laser Therapy - SLT as First-Line | Selective Laser Trabeculoplasty (SLT) | LiGHT trial established SLT as a safe, effective first-line therapy for OAG/OHT, with 74% of patients medication-free at 3 years. GLAUrious trial (2025) confirmed non-inferiority vs. drops as primary treatment. Low blister-formation risk; repeatable. | Established; now recommended first-line by many guidelines | Jayaram et al., Lancet 2023 [PMID 37742700]; PMC12460366 |
| Laser Therapy - Micropulse | Micropulse Transscleral Laser Therapy (TLT) | Cyclophotocoagulation with sub-threshold micropulse energy; less collateral tissue damage compared to continuous-wave CPC. Useful in refractory glaucoma. | In clinical use | PMC12460366 |
| MIGS - Schlemm's Canal | iStent inject W, Hydrus Microstent | Trabecular bypass/scaffold devices placed ab interno. Hydrus shown to maintain IOP reduction and reduce medication use long-term in pivotal trials. Used with or without cataract surgery. | FDA-approved; widely used | Balas & Mathew, Vision 2023 [PMID 37606500]; Chihara & Hamanaka, J Clin Med 2024 [PMID 39201024] |
| MIGS - Schlemm's Canal | Canaloplasty (ABiC/OMNI) | Ab interno canaloplasty distends Schlemm's canal and collector channels; OMNI system combines goniotomy with canaloplasty. Growing evidence in normal-tension glaucoma. | FDA-approved; in clinical use | Wagner et al., J Curr Glaucoma Pract 2024 [PMID 39144728]; Oo et al., Clin Exp Ophthalmol 2024 [PMID 38853535] |
| MIGS - Supraciliary/Uveoscleral | Alloflo Uveo (Iantrek) | Supraciliary micro-stent targeting uveoscleral outflow via negative pressure gradient in the supraciliary space. Recently FDA-approved. For moderate disease not severe enough for bleb surgery. | Recently FDA-approved | 2026 Glaucoma Pipeline |
| MIGS - Subconjunctival Bleb | PRESERFLO MicroShunt, XEN Gel Stent | Ab interno bleb-forming devices creating subconjunctival drainage. Lower complication profiles compared to trabeculectomy; less hypotony risk. | FDA-approved / CE-marked | Balas & Mathew, Vision 2023 [PMID 37606500] |
| MIGS - Novel Devices | Minimally Invasive Micro Sclerostomy (MIMS) | Creates a micro-sclerostomy without conjunctival incision; 12-month data published 2024 in BMC Ophthalmol. | Published phase studies (2024) | 2026 Glaucoma Pipeline |
| MIGS - Novel Devices | Aqualumen (PLU Ophthalmic) | 22-gauge transconjunctival device creating a tunnel from the anterior chamber to the subconjunctival space - forms a bleb without opening the eye. FDA Class I device. | Recently available (US) | 2026 Glaucoma Pipeline |
| MIGS - Novel Devices | MINIject (iSTAR Medical) | Suprachoroidal soft implant; STAR-GLOBAL trial demonstrated significant sustained IOP reduction at 5 years. | 5-year trial data (2025) | 2026 Glaucoma Pipeline |
| Neuroprotection | Brimonidine (neuroprotective role) | Alpha-2 agonist with proven IOP-lowering and possible neuroprotective effects on retinal ganglion cells via BDNF upregulation. Under further investigation. | Established drug; neuroprotection under study | Jayaram et al., Lancet 2023 [PMID 37742700] |
| Neuroprotection - Cell Therapy | NT-501 / Encelto (Neurotech) | Encapsulated cell-based intravitreal implant releasing ciliary neurotrophic factor (CNTF) continuously, promoting retinal ganglion cell survival. Approved 2025 for macular telangiectasia (Encelto); Phase 2 trials ongoing for glaucoma. | Phase 2 for glaucoma; FDA-approved for another indication (2025) | 2026 Glaucoma Pipeline |
| Neuroprotection - Gene Therapy | Astrocyte-targeting gene therapy | Stanford research (2024, Nature) identified a gene therapy that converts harmful astrocytes to a neuroprotective phenotype in mouse models, preventing RGC damage even at normal IOP. | Preclinical (mouse model, 2024) | Stanford Medicine |
| Neuroprotection - Gene Therapy | IOP-independent RGC neuroprotection | Multiple approaches in early-phase trials: CNTF delivery, BDNF, mTOR pathway activation (PTEN deletion), Wnt signaling modulation to promote RGC axon survival and regeneration. | Preclinical / early Phase 1-2 | Lee et al., Curr Opin Pharmacol 2024 [PMID 38171063]; Jayaram et al., Lancet 2023 [PMID 37742700] |
| Personalized / Precision Medicine | Genetic risk profiling | Identification of risk loci (MYOC, OPTN, TBK1, NTF4, WDR36) enables genetic screening for early detection and personalized treatment. AI integration for risk stratification is in active development. | Research / emerging clinical use | Jayaram et al., Lancet 2023 [PMID 37742700] |
| AI & Diagnostics | AI-assisted detection and progression monitoring | Deep learning models for optic disc analysis, OCT RNFL automated progression detection, and glaucoma screening from fundus photos. Improves sensitivity in under-resourced settings. | Emerging clinical integration | Jayaram et al., Lancet 2023 [PMID 37742700] |
| Fixed-Dose Combinations | New combination drops | Netarsudil/latanoprost (Rocklatan), bimatoprost/timolol, dorzolamide/timolol - improve adherence. Dual or triple mechanism approaches are expanding. MIMS combining two novel agents (e.g., ROCK + PGA) in development. | In clinical use / pipeline | PMC12460366 |
Make a short note for pg ophthalmology exam on the topic role of AI in ophthalmology
artificial intelligence ophthalmology deep learning retina glaucoma diabetic retinopathy
role of artificial intelligence in ophthalmology 2024 2025 exam review applications
https://eyewiki.org/Artificial_Intelligence_in_Ophthalmology
| Condition | AI Application | Key Milestone |
|---|---|---|
| Diabetic Retinopathy (DR) | Autonomous fundus photo screening for referable DR | IDx-DR (now LumineticsCore) - first FDA-authorized autonomous AI system for DR screening (2018) |
| Diabetic Macular Edema (DME) | OCT-based fluid segmentation, quantification, treatment-response prediction | Multiple FDA-cleared tools in clinical use |
| Age-Related Macular Degeneration (AMD) | Detection of drusen, geographic atrophy, CNV on OCT and fundus | DeepMind (Google) AI matches expert retinal specialists in diagnosis |
| Retinal Vascular Occlusions | Automated classification and systemic risk factor correlation | Active research phase |
Exam Point: IDx-DR / LumineticsCore was the first FDA-cleared autonomous (no ophthalmologist required) AI diagnostic system - approved 2018 for DR screening.
Exam Point: AI-based IOL formulas (Hill-RBF, Kane) are now preferred over traditional formulas (Haigis, Hoffer Q, SRK/T) in complex eyes.
Exam Point: ROP AI screening is highly relevant in India due to shortage of trained ROP screeners in tier-2/3 hospitals.
| Year | Milestone |
|---|---|
| 2018 | IDx-DR - first FDA-cleared autonomous AI diagnostic device (ophthalmology) |
| 2020 | EyeArt - FDA cleared for autonomous DR screening |
| 2021 | LumineticsCore (rebranded IDx-DR) - updated clearance |
| 2023-25 | Multiple OCT-based AI tools for AMD, DR fluid quantification cleared |
| Fact | Answer |
|---|---|
| First FDA-cleared autonomous AI ophthalmic device | IDx-DR (LumineticsCore) - 2018, for DR |
| Best studied subspecialty for AI | Retina (specifically DR screening) |
| AI in IOL calculation | Hill-RBF, Kane formula - superior to SRK/T in complex cases |
| AI in glaucoma | Decision-support only; no autonomous tool yet |
| AI for ROP in India | KIDROP, i-RET telemedicine platform |
| Technology used in most ophthalmic AI | Convolutional Neural Networks (CNN) / Deep Learning |
| Retinal AI detecting systemic disease | Cardiovascular risk, CKD, anaemia, Alzheimer's biomarkers |
| Limitation of AI | Bias, black box, regulatory lag, equity concerns |