Extended Intraocular Drug-Delivery Platforms for the Treatment of Retinal and Choroidal Diseases

Author:

Wykoff Charles C.1ORCID,Kuppermann Baruch D.2,Regillo Carl D.3,Chang Margaret4,Hariprasad Seenu M.5,Duker Jay S.67,Altaf Syed6,Saïm Saïd6

Affiliation:

1. Retina Consultants of Texas; Retina Consultants of America; Blanton Eye Institute, Houston, Methodist Hospital, Houston, TX, USA

2. Gavin Herbert Eye Institute, University of California, Irvine, CA, USA

3. Mid Atlantic Retina, Wills Eye Hospital Retina Service, Thomas Jefferson University, Philadelphia, PA, USA

4. Retinal Consultants Medical Group, Sacramento, CA, USA

5. University of Chicago, Department of Ophthalmology and Visual Science, Chicago, IL, USA

6. EyePoint Pharmaceuticals, Watertown, MA, USA

7. New England Eye Center, Tufts University, Boston, MA, USA

Abstract

Purpose: To review sustained-release intraocular platforms used to treat diseases of the retina and choroid. Methods: A literature review of the current applications of biomaterials for sustained-release therapy in retinal and choroidal diseases was performed. Results: Retinal and choroidal diseases, such as neovascular age-related macular degeneration (nAMD), diabetic retinopathy (DR), diabetic macular edema (DME), and uveitis, are commonly treated using intravitreal (IVT) therapies that require frequent IVT injections. Multiple sustained-release options for IVT therapy have been approved by the US Food and Drug Administration for the treatment of inflammatory eye diseases, including noninfectious uveitis, infectious diseases, and exudative retinal diseases (eg, retinal venous occlusive disease and DME) using drugs such as fluocinolone acetonide, ganciclovir, and dexamethasone. The platforms for these drugs are biodegradable or nonbiodegradable. They use biomaterials such as polymers and hydrogels and are typically implanted surgically or injected into the vitreous, where they release the drug gradually over months or years. Building on these technologies, novel platforms are being studied that are intended to treat conditions including nAMD, DR, DME, and uveitis. These platforms are being tested for their safety, efficacy, and ability to reduce the injection and visit burden. Conclusions: Multiple sustained-release ocular drug-delivery platforms are currently commercially available, and many new sustained-release IVT platforms are being investigated. The hope is that meaningfully reducing the injection burden by extending intervals between treatments while maintaining optimal efficacy will improve long-term outcomes.

Funder

EyePoint Pharmaceuticals

Publisher

SAGE Publications

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