PUBLISHER: Mordor Intelligence | PRODUCT CODE: 1852206
PUBLISHER: Mordor Intelligence | PRODUCT CODE: 1852206
The macular degeneration treatment market size is USD 16.79 billion in 2025 and is projected to reach USD 25.25 billion by 2030, advancing at an 8.51% CAGR.

The outlook reflects demographic aging, regulatory support for breakthrough drugs, and rapid diffusion of digital diagnostics that identify disease earlier than conventional eye-care pathways. Elevated demand is reinforced by the 25% faster-than-aging rise in age-related macular degeneration (AMD) prevalence, the 94% sensitivity and 99% specificity of AI-based screening algorithms, and the pivot to complement pathway inhibitors that open therapy options for geographic atrophy. Gene and cell therapies in late-stage trials, sustained-release delivery platforms, and biosimilar price competition are reshaping revenue streams even as payers tighten utilization controls to contain biologic costs. Regionally, the United States retains first-mover access to novel treatments by leveraging the FDA's breakthrough-therapy channel, while Asia-Pacific's accelerating reimbursement expansion and massive elderly cohort underpin the fastest unit growth.
AMD prevalence is outpacing baseline aging trends by 25% as lifestyle factors such as prolonged screen time, poor diet quality, and rising urban pollution compound hereditary risks. WHO projects 288 million people living with AMD by 2030, pushing health systems toward earlier detection protocols that enlarge the treatable population by 40% relative to clinic-based screening. Untreated AMD already drains USD 343 billion in global productivity and care costs, spurring insurers to endorse preventive regimens including regular imaging and nutritional support. Nations with mature diagnostic networks are witnessing steep adoption of AI-enabled screening that reaches primary-care settings and pharmacies, effectively re-routing patients into therapy pipelines sooner. Pharmaceutical companies are responding with extended-duration implants that align with proactive care models and reduce office-visit congestion.
Individuals aged >= 65 will represent 16.5% of humanity by 2030, and the 85+ cohort-most vulnerable to advanced AMD-is expanding at twice the broader elderly growth rate. Asia-Pacific nations led by Japan and South Korea are confronting unprecedented demand that strains specialist availability and catalyzes tele-ophthalmology adoption. Elderly patients often carry comorbid diabetes or hypertension, complicating anti-VEGF injection regimens and mandating closer safety oversight. U.S. Medicare spending on anti-VEGF therapy climbed from USD 2.51 billion in 2014 to USD 4.02 billion in 2019; projections show another doubling by 2030 absent less costly options. Governments thus favor self-administered agents and home-monitoring devices that cushion capacity bottlenecks and temper budget escalation.
Leading anti-VEGF injections are priced at USD 1,850-2,000 per dose, and typical regimens of 6-8 injections per year can exceed USD 15,000 before diagnostics and physician fees. One-time gene therapies under development may demand USD 200,000-500,000 per eye, igniting payer scrutiny despite potential lifetime cost offsets. Aflibercept biosimilars launched in 2024 shave 15-30% off list prices, yet switching inertia and product-specific safety data gaps curb rapid penetration. Payers are responding with step-therapy rules, site-of-care restrictions, and outcomes-based contracting pilots that tie reimbursement to visual-acuity durability. These access frictions temper near-term uptake of high-priced modalities and could drag the macular degeneration treatment market CAGR by nearly two percentage points.
Other drivers and restraints analyzed in the detailed report include:
For complete list of drivers and restraints, kindly check the Table Of Contents.
Wet AMD's 65.43% 2024 revenue dominance demonstrates the entrenchment of anti-VEGF therapy, yet growth deceleration is evident as biosimilars erode price and volume share. Trajectory shifts favor the dry-AMD segment, where SYFOVRE and IZERVAY approvals generated the first pharmacologic options for geographic atrophy, cutting lesion-expansion by up to 35%. As real-world data validate safety, payer adoption accelerates, propelling a 10.43% CAGR that reshapes portfolio priorities across the macular degeneration treatment market. Gene-therapy researchers concentrate disproportionately on dry AMD, attracted by a patient pool that comprises roughly 85% of total AMD cases and the opportunity to deliver one-time treatments that could circumvent lifelong injections.
Competitive investment now skews toward complement modulation and photoreceptor protection, with Phase III readouts expected across multiple mechanisms by 2027. Leading incumbents staunch wet-AMD share loss through high-dose aflibercept and combined VEGF/Ang-2 suppression, but strategic capital increasingly shifts to dry-AMD assets via acquisition and co-development deals. Commercial analysts anticipate convergence of wet and dry revenue lines by 2029 if dry-segment uptake maintains current velocity, a milestone that would recalibrate valuation metrics across the macular degeneration treatment industry.
Early-stage AMD accounted for 72.43% of the 2024 macular degeneration treatment market size, reflecting diagnostic expansion into primary-care, optometry, and community-pharmacy channels through cloud-connected fundus cameras. Ophthalmic societies endorse AREDS-based supplementation and lifestyle adjustments for newly diagnosed patients, anchoring a preventive-care economy that supports nutraceutical manufacturers and tele-monitoring vendors. Intermediate-stage AMD boasts the fastest segment CAGR at 10.99% through 2030 as complement inhibitors demonstrate lesion-growth suppression and extend "functional vision years" for patients. The commercial narrative emphasizes halting progression rather than restoring lost acuity, aligning payer interest with societal cost-avoidance.
Late-stage AMD remains the highest per-patient revenue tier because of recurring injection schedules and assistive-device demand. Nonetheless, sustained-release implants and gene therapies threaten to compress visit volumes and disrupt traditional fee-for-service business models. Real-time home-OCT devices streamline triage, routing only deteriorating eyes into clinic for prompt rescue, conserving capacity and advancing precision medicine across the macular degeneration treatment market.
The Macular Degeneration Treatment Market Report is Segmented by Disease Form (Dry Age-Related Macular Degeneration and Wet Age-Related Macular Degeneration), Stage of Disease (Early-Stage AMD, and More), Treatment Type (Drugs, and Surgery), Route of Administration (Intravitreal, and More), Sales Channels (Hospitals, and More), and Geography (North America, and More). The Market Forecasts are Provided in Terms of Value (USD).