This audio article is from VisualFieldTest.com.
Read the full article here: https://visualfieldtest.com/en/glaucoma-vision-restoration-what-s-new-in-january-2026
Test your visual field online: https://visualfieldtest.com
Support the show so new episodes keep coming: https://www.buzzsprout.com/2563091/support
Excerpt:
Glaucoma Vision Restoration: What’s New in January 2026Glaucoma is often called the “silent thief of sight” – a group of eye diseases where damage to the optic nerve leads to permanent vision loss. Current treatments can only slow glaucoma by lowering eye pressure; they do not restore lost vision. But exciting research is now aiming to repair or replace the damaged retinal ganglion cells and optic nerve fibers. In the past few years, scientists have reported many breakthrough approaches. These include new neuroprotective therapies to shield surviving cells, gene therapies that could make nerve cells regenerate, stem-cell treatments to replace lost neurons, and even optogenetic or bionic-vision strategies to bypass damaged tissue. Although these ideas are mostly experimental, early news is encouraging. In late 2025, for example, a clinical trial kicked off to “rejuvenate” optic nerve cells with gene therapy () – sparking hope that glaucoma vision loss might one day be reversed. Other teams have reported partial vision returns in blind patients using implanted electronics or light-sensitive proteins () (). This article reviews the state of regenerative ophthalmology for glaucoma as of early 2026. We explain the new therapies under study, summarize any recent trial results or regulatory news, and give a realistic sense of how far these advances are from helping patients. (In short, there’s promise, but practical cures are still years away () ().) Read on for the latest on each approach.Neuroprotective TherapiesOne major strategy is neuroprotection, which means using drugs or treatments to keep surviving retinal ganglion cells (RGCs) alive and healthy longer. The idea is to slow or stop cell death so patients lose vision more slowly and perhaps maintain useful sight. Researchers are exploring many ways to do this:Growth factors and cytokines. Delivering nerve-growth substances such as brain-derived neurotrophic factor (BDNF), ciliary neurotrophic factor (CNTF), or other supportive proteins into the eye. These molecules can help RGCs resist stress and avoid programmed cell death. For example, implantable devices have been tested that slowly release CNTF in the retina, with some evidence they protect retinal cells. (No neuroprotective drug for glaucoma is yet FDA-approved, but dozens of compounds are under study.) Anti-inflammatory and antioxidant approaches. Chronic inflammation and oxidative stress contribute to glaucoma damage. Some experimental treatments aim to block those pathways – for example by shutting down inflammatory signals or scavenging free radicals in the optic nerve head. These too are still in research stages. Pressure-independent medicines. Interestingly, some glaucoma drugs known to lower eye pressure may also have direct neuroprotective properties. For instance, the drug brimonidine (an eye-drop alpha-agonist) has been studied for neuroprotection, though results in trials have been mixed. Similarly, new Rho kinase inhibitors (like netarsudil) are being reviewed not only for pressure-lowering but also for possible nerve-protecting effects.So far, neuroprotection remains a concept rather than a clinically proven therapy. As Dr. Joseph Rizzo (Harvard Ophthalmology) notes, one compelling idea is simply to “make the cell
