VEGF Inhibitors Therapeutic for Diabetic Retinopathy Market Research Report with Forecast 2025 to 2034

Report Id: 3088 Pages: 160 Last Updated: 17 December 2025 Format: PDF / PPT / Excel / Power BI
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VEGF Inhibitors Therapeutic for Diabetic Retinopathy Market Size is predicted to expand with a 6.8% CAGR during the forecast period for 2025 to 2034.

VEGF Inhibitors Therapeutic for Diabetic Retinopathy Market, Share & Trends Analysis Report, By Drug Type (Aflibercept, Ranibizumab, Bevacizumab, Faricimab, Biosimilars, Pipeline drugs), By Indication (Diabetic Macular Edema (DME), Proliferative. Diabetic Retinopathy (PDR), Non-Proliferative Diabetic Retinopathy (NPDR)), By Delivery Method, By Region, and Segment Forecasts, 2025 to 2034 

VEGF Inhibitors Therapeutic for Diabetic Retinopathy Market

Inhibitors of VEGF (Vascular Endothelial Growth Factor) are a standard treatment for diabetic retinopathy, particularly in cases of proliferative diabetic retinopathy (PDR) and diabetic macular edema (DME). These medications function by targeting VEGF, a protein that promotes the formation of abnormal blood vessels and increases vascular permeability in the retina, two key mechanisms underlying the progression of diabetic retinopathy. Elevated VEGF levels in the diabetic retina led to neovascularization, increased vascular leakage, causing macular edema, and progressive retinal damage, which can result in vision loss. By blocking VEGF activity, these inhibitors prevent the growth of abnormal blood vessels, reduce fluid leakage and retinal swelling, and ultimately help to stabilize or even improve visual acuity in affected patients.

Ranibizumab, a vascular endothelial growth factor (VEGF) inhibitor, is a key treatment for diabetic retinopathy, including diabetic macular edema (DME). It works by inhibiting the formation of abnormal new blood vessels and reducing fluid leakage in the retina, two hallmark features of diabetic retinopathy. Ranibizumab is a recombinant humanized monoclonal antibody fragment that selectively binds to VEGF-A, a protein that promotes angiogenesis, thereby effectively suppressing disease progression. Alongside ranibizumab, other VEGF inhibitors such as aflibercept, bevacizumab, and faricimab have demonstrated strong clinical efficacy in reducing macular edema and improving or stabilizing vision. Growing emphasis on early detection and treatment, supported by advancements in non-invasive imaging and teleophthalmology, further supports the expanding role of anti-VEGF therapies in the management of diabetic retinopathy.

Competitive Landscape

Some of the Major Key Players in the VEGF Inhibitors Therapeutic for Diabetic Retinopathy Market are:

  • Regeneron Pharmaceuticals, Inc.
  • Hoffmann-La Roche Ltd.
  • Novartis AG
  • Bayer AG
  • Genentech, Inc. (Roche subsidiary)
  • Kodiak Sciences Inc.
  • Innovent Biologics, Inc.
  • Ashvattha Therapeutics, Inc.
  • UNITY Biotechnology, Inc.
  • PanOptica, Inc.
  • Regenxbio Inc.
  • Ocular Therapeutix, Inc.
  • Adverum Biotechnologies, Inc

Market Segmentation

The VEGF inhibitors therapeutic for the diabetic retinopathy market is segmented based on drug type, indication, and delivery method. Based on Drug Type, the market is segmented into aflibercept, ranibizumab, bevacizumab, faricimab, biosimilars, and pipeline drugs. Based on the Indication, the market is divided into diabetic macular edema (DME), proliferative. diabetic retinopathy (PDR), non-proliferative diabetic retinopathy (NPDR). Based on the delivery method, the market is divided into intravitreal injections, sustained-release implants, and emerging technologies.

The Aflibercept (Eylea) Segment is Expected to Have the Highest Growth Rate During the Forecast Period.

Based on Drug Type, the market is segmented into aflibercept, ranibizumab, bevacizumab, faricimab, biosimilars, and pipeline drugs. the aflibercept (Eylea) segment is expected to have the highest growth rate during the forecast period. Eylea has demonstrated strong clinical efficacy in stabilizing and improving vision in patients with retinal diseases. It is approved for multiple indications, including wet age-related macular degeneration (AMD), DME, and diabetic retinopathy, making it a versatile treatment option. The introduction of Eylea HD, an 8 mg high-dose formulation, allows for longer intervals between injections (up to 16 weeks), reducing the treatment burden on patients and healthcare providers. 

The Non-Proliferative Diabetic Retinopathy (NPDR) Segment Dominates the Market

Based on the Indication, the market is divided into diabetic macular edema (DME), proliferative. diabetic retinopathy (PDR), non-proliferative diabetic retinopathy (NPDR). Among these, the non-proliferative diabetic retinopathy (NPDR) segment dominates the market.  There's a growing emphasis on early detection and treatment of diabetic retinopathy. Initiating anti-VEGF therapy during the NPDR stage can prevent progression to more severe forms, such as Proliferative Diabetic Retinopathy (PDR) and Diabetic Macular Edema (DME). Studies have demonstrated that early treatment of severe NPDR with anti-VEGF agents leads to a significant reduction in the risk of progression to PDR.

North America Has the Largest Market Share During the Forecast Period.

The North America region particularly the United States, holds the largest share of the VEGF Inhibitors Therapeutic for Diabetic Retinopathy Market during the forecast period. North America boasts a well-developed healthcare system with widespread access to eye care specialists and advanced diagnostic technologies, which facilitates the early detection and effective treatment of diabetic retinopathy.

The United States, in particular, has a significant diabetic population, contributing to a higher incidence of diabetic retinopathy and a corresponding increase in demand for targeted therapies. Additionally, the region has demonstrated rapid adoption of innovative treatments, including anti-VEGF agents, driven by robust clinical research infrastructure and timely regulatory approvals. These factors collectively support North America's leading position in the VEGF inhibitors therapeutic market for diabetic retinopathy.

Recent Developments:

  • In March 2025, Kodiak Sciences Inc. declared that it has finished enrolling patients with diabetic retinopathy ("DR") in its GLOW2 Phase 3 clinical trial of tarcocimab tedromer. " With the added benefit of an extra loading dosage to give physicians more dosing options, the GLOW2 design is similar to the successful GLOW1 research. They expect to have a regulatory package for tarcocimab that is prepared for filing if the results of GLOW2, the second registrational study in diabetic retinopathy, are favorable.
  • In July 2024, Genentech, a member of the Roche Group, revealed two-year results from the Phase III Pagoda and Pavilion trials, which assessed Susvimo® (ranibizumab injection) 100 mg/mL for the treatment of diabetic retinopathy (DR) and diabetic macular edema (DME), the two main conditions that cause vision loss in diabetic people. The first and only refillable eye implant that uses the Port Delivery Platform to continuously supply a tailored ranibizumab formulation is Susvimo.

VEGF Inhibitors Therapeutic for Diabetic Retinopathy Market Report Scope:

Report Attribute Specifications
Growth Rate CAGR CAGR of 6.8% from 2025 to 2034
Quantitative Units Representation of revenue in US$ Mn and CAGR from 2025 to 2034
Historic Year 2021 to 2024
Forecast Year 2025-2034
Report Coverage The forecast of revenue, the position of the company, the competitive market structure, growth prospects, and trends
Segments Covered By Drug Type, Indication, Delivery Method
Regional Scope North America; Europe; Asia Pacific; Latin America; Middle East & Africa
Country Scope U.S.; Canada; U.K.; Germany; China; India; Japan; Brazil; Mexico; The UK; France; Italy; Spain; China; Japan; India; South Korea; Southeast Asia; South Korea; South East Asia
Competitive Landscape Regeneron Pharmaceuticals, Inc, F. Hoffmann-La Roche Ltd, Novartis AG, Bayer AG, Genentech, Inc. (Roche subsidiary), Kodiak Sciences Inc, Innovent Biologics, Inc, Ashvattha Therapeutics, Inc, UNITY Biotechnology, Inc, PanOptica, Inc, Regenxbio Inc. Ocular Therapeutix, Inc, Adverum Biotechnologies, Inc.
Customization Scope Free customization report with the procurement of the report and modifications to the regional and segment scope. Particular Geographic competitive landscape.
Pricing and Available Payment Methods Explore pricing alternatives that are customized to your particular study requirements.

Segmentation of VEGF Inhibitors Therapeutic for Diabetic Retinopathy Market

Global VEGF Inhibitors Therapeutic for Diabetic Retinopathy Market - By Drug Type

  • Aflibercept (Eylea)
  • Ranibizumab (Lucentis)
  • Bevacizumab (Avastin, off-label)
  • Faricimab (Vabysmo, dual VEGF/Ang-2 inhibitor)
  • Biosimilars
  • Pipeline drugs

VEGF Inhibitors Therapeutic for Diabetic Retinopathy Market

Global VEGF Inhibitors Therapeutic for Diabetic Retinopathy Market – By Indication

  • Diabetic Macular Edema (DME)
  • Proliferative Diabetic Retinopathy (PDR)
  • Non-Proliferative Diabetic Retinopathy (NPDR)

Global VEGF Inhibitors Therapeutic for Diabetic Retinopathy Market – By Delivery Method

  • Intravitreal Injections
  • Sustained-Release Implants
  • Emerging

Global VEGF Inhibitors Therapeutic for Diabetic Retinopathy Market – By Region

North America-

  • The US
  • Canada

Europe-

  • Germany
  • The UK
  • France
  • Italy
  • Spain
  • Rest of Europe

Asia-Pacific-

  • China
  • Japan
  • India
  • South Korea
  • Southeast Asia
  • Rest of Asia Pacific

Latin America-

  • Brazil
  • Argentina
  • Mexico
  • Rest of Latin America

 Middle East & Africa-

  • GCC Countries
  • South Africa
  • Rest of the Middle East and Africa

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Research Design and Approach

This study employed a multi-step, mixed-method research approach that integrates:

  • Secondary research
  • Primary research
  • Data triangulation
  • Hybrid top-down and bottom-up modelling
  • Forecasting and scenario analysis

This approach ensures a balanced and validated understanding of both macro- and micro-level market factors influencing the market.

Secondary Research

Secondary research for this study involved the collection, review, and analysis of publicly available and paid data sources to build the initial fact base, understand historical market behaviour, identify data gaps, and refine the hypotheses for primary research.

Sources Consulted

Secondary data for the market study was gathered from multiple credible sources, including:

  • Government databases, regulatory bodies, and public institutions
  • International organizations (WHO, OECD, IMF, World Bank, etc.)
  • Commercial and paid databases
  • Industry associations, trade publications, and technical journals
  • Company annual reports, investor presentations, press releases, and SEC filings
  • Academic research papers, patents, and scientific literature
  • Previous market research publications and syndicated reports

These sources were used to compile historical data, market volumes/prices, industry trends, technological developments, and competitive insights.

Secondary Research

Primary Research

Primary research was conducted to validate secondary data, understand real-time market dynamics, capture price points and adoption trends, and verify the assumptions used in the market modelling.

Stakeholders Interviewed

Primary interviews for this study involved:

  • Manufacturers and suppliers in the market value chain
  • Distributors, channel partners, and integrators
  • End-users / customers (e.g., hospitals, labs, enterprises, consumers, etc., depending on the market)
  • Industry experts, technology specialists, consultants, and regulatory professionals
  • Senior executives (CEOs, CTOs, VPs, Directors) and product managers

Interview Process

Interviews were conducted via:

  • Structured and semi-structured questionnaires
  • Telephonic and video interactions
  • Email correspondences
  • Expert consultation sessions

Primary insights were incorporated into demand modelling, pricing analysis, technology evaluation, and market share estimation.

Data Processing, Normalization, and Validation

All collected data were processed and normalized to ensure consistency and comparability across regions and time frames.

The data validation process included:

  • Standardization of units (currency conversions, volume units, inflation adjustments)
  • Cross-verification of data points across multiple secondary sources
  • Normalization of inconsistent datasets
  • Identification and resolution of data gaps
  • Outlier detection and removal through algorithmic and manual checks
  • Plausibility and coherence checks across segments and geographies

This ensured that the dataset used for modelling was clean, robust, and reliable.

Market Size Estimation and Data Triangulation

Bottom-Up Approach

The bottom-up approach involved aggregating segment-level data, such as:

  • Company revenues
  • Product-level sales
  • Installed base/usage volumes
  • Adoption and penetration rates
  • Pricing analysis

This method was primarily used when detailed micro-level market data were available.

Bottom Up Approach

Top-Down Approach

The top-down approach used macro-level indicators:

  • Parent market benchmarks
  • Global/regional industry trends
  • Economic indicators (GDP, demographics, spending patterns)
  • Penetration and usage ratios

This approach was used for segments where granular data were limited or inconsistent.

Hybrid Triangulation Approach

To ensure accuracy, a triangulated hybrid model was used. This included:

  • Reconciling top-down and bottom-up estimates
  • Cross-checking revenues, volumes, and pricing assumptions
  • Incorporating expert insights to validate segment splits and adoption rates

This multi-angle validation yielded the final market size.

Forecasting Framework and Scenario Modelling

Market forecasts were developed using a combination of time-series modelling, adoption curve analysis, and driver-based forecasting tools.

Forecasting Methods

  • Time-series modelling
  • S-curve and diffusion models (for emerging technologies)
  • Driver-based forecasting (GDP, disposable income, adoption rates, regulatory changes)
  • Price elasticity models
  • Market maturity and lifecycle-based projections

Scenario Analysis

Given inherent uncertainties, three scenarios were constructed:

  • Base-Case Scenario: Expected trajectory under current conditions
  • Optimistic Scenario: High adoption, favourable regulation, strong economic tailwinds
  • Conservative Scenario: Slow adoption, regulatory delays, economic constraints

Sensitivity testing was conducted on key variables, including pricing, demand elasticity, and regional adoption.

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Frequently Asked Questions

VEGF Inhibitors Therapeutic for Diabetic Retinopathy Market Size is predicted to expand with a 6.8% CAGR during the forecast period for 2025 to 2034

Regeneron Pharmaceuticals, Inc, F. Hoffmann-La Roche Ltd, Novartis AG, Bayer AG, Genentech, Inc. (Roche subsidiary), Kodiak Sciences Inc, Innovent Bio

Drug Type, Indication and Delivery Method are the key segments of the VEGF Inhibitors Therapeutic for Diabetic Retinopathy Market.

North America region is leading the VEGF Inhibitors Therapeutic for Diabetic Retinopathy Market.
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