DelveInsight’s "Retinal Vein Occlusion Pipeline Insight 2025" report delivers an in-depth examination of more than 15 pharmaceutical organizations and their 15+ investigational therapies currently advancing within the Retinal Vein Occlusion (RVO) research and development landscape. The study encompasses comprehensive profiles of both clinical and preclinical pipeline assets, with thorough evaluation across product classification, stage of development, route of administration, and molecular type. It also identifies inactive or discontinued therapeutic programs within this area.
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On October 3, 2025, EyeBiotech Ltd. initiated a multi-cohort study involving four patient groups, each randomized (1:1) to receive either a low or high dose of EYE103 through intravitreal (IVT) injection. A total of 40 participants per cohort will be enrolled, with sequential enrollment guided by the sponsor’s discretion.
According to DelveInsight’s findings, the Retinal Vein Occlusion market features over 15 active developers advancing novel therapeutic formulations.
Leading pharmaceutical participants include Kodiak Sciences, Hoffman-La-Roche, iRenix Medical Inc., Sunshine Guojian Pharmaceutical, Ripple Therapeutics, Aerpio Therapeutics, The Emmes Company, Novartis, Shanghai BDgene, AsclepiX Therapeutics, Taiwan Liposome Company, Clearside Biomedical, Gene Signal, Ocular Therapeutix, Ocuphire Pharma, and Eyevensys.
Notable therapies in development encompass Aflibercept Injection (EYLEA, VEGF Trap-Eye, BAY86-5321), Sham Treatment, Macular Laser Photocoagulation, Faricimab, and others.
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Retinal vein occlusion ranks as the second most common retinal vascular disorder, representing a leading cause of vision impairment among elderly individuals. It is categorized into two primary types: Branch Retinal Vein Occlusion (BRVO) and Central Retinal Vein Occlusion (CRVO). CRVO—resulting from thrombosis of the main retinal vein posterior to the lamina cribrosa—can be further subdivided into ischemic (nonperfused) and non-ischemic (perfused) forms.
KSI-301 (Kodiak Sciences):
A next-generation anti-VEGF biologic engineered for prolonged intraocular activity. KSI-301 aims to reduce treatment frequency while sustaining efficacy, thereby alleviating injection burden on patients and providers. The therapy is currently under Phase III evaluation for RVO.
601 (Sunshine Guojian Pharmaceutical):
A recombinant humanized anti-VEGF monoclonal antibody injection being studied for retinal conditions including age-related macular degeneration, diabetic macular edema, and RVO. It is presently undergoing Phase II clinical trials.
IBE-814 (Ripple Therapeutics):
Formulated to deliver consistent steroid dosing over six to nine months, IBE-814 seeks to enhance clinical benefits and minimize common steroid-related side effects. The RIPPLE-1 Phase II study evaluates safety and efficacy of differing IBE-814 IVT regimens for macular edema secondary to RVO.
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The report offers an analytical view of key pharmaceutical developers engaged in RVO therapy innovation, segmented by their developmental phase—early, mid, and late stages. It also maps each company’s active, inactive, and discontinued projects. Insights include investigational drug targeting, mechanisms of action, monotherapy versus combination therapy status, and molecular attributes.
Additionally, DelveInsight examines partnership structures, academic collaborations, licensing agreements, and capital investments propelling future RVO market expansions.
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Entities leading research and pipeline activity include Kodiak Sciences, Hoffman-La-Roche, iRenix Medical Inc., Sunshine Guojian Pharmaceutical, Ripple Therapeutics, Aerpio Therapeutics, The Emmes Company, Novartis, Shanghai BDgene, AsclepiX Therapeutics, Taiwan Liposome Company, Clearside Biomedical, Gene Signal, Ocular Therapeutix, Ocuphire Pharma, and Eyevensys.
RVO pipeline products are classified by administration pathway:
Oral
Parenteral
Intravitreal
Subretinal
Topical
Therapies are differentiated by molecule type:
Monoclonal Antibody
Peptide
Polymer
Small Molecule
Gene Therapy
Coverage: Global
Companies Covered: Kodiak Sciences, Hoffman-La-Roche, iRenix Medical, Sunshine Guojian Pharmaceutical, Ripple Therapeutics, Aerpio Therapeutics, Novartis, Shanghai BDgene, AsclepiX Therapeutics, Taiwan Liposome Company, Clearside Biomedical, Ocular Therapeutix, Ocuphire Pharma, Eyevensys, and others.
Key Therapies: EYLEA (Aflibercept), Faricimab, Macular Laser Photocoagulation, and other emerging anti-VEGF and corticosteroid candidates.
Therapeutic Assessments: Conducted by product type (Mono, Combination, or Mixed), by clinical stage (Discovery to Phase III), and by route of administration.
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Introduction
Executive Summary
Retinal Vein Occlusion: Overview
Pipeline Therapeutics
Therapeutic Assessment
Late Stage Products (Phase III)
KSI-301: Kodiak Sciences
Mid Stage Products (Phase II)
601: Sunshine Guojian Pharmaceutical
Early Stage Products (Phase I)
MHU650: Novartis
Inactive Products
Retinal Vein Occlusion Key Companies
Retinal Vein Occlusion Key Products
Retinal Vein Occlusion- Unmet Needs
Retinal Vein Occlusion- Market Drivers and Barriers
Retinal Vein Occlusion- Future Perspectives and Conclusion
Retinal Vein Occlusion Analyst Views
Retinal Vein Occlusion Key Companies
Appendix
DelveInsight is a global healthcare market intelligence and consulting firm offering extensive analytical capabilities across the life sciences spectrum. With expert researchers and a focus on clinical innovation, DelveInsight provides custom-tailored insights to enable strategic business decisions for pharmaceutical, biotech, and healthcare organizations worldwide.
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