Types segmentation classifies anti‑VEGF agents according to molecular architecture and regulatory status, a key determinant of market dynamics. Ranibizumab, a Fab fragment engineered for high ocular affinity, holds roughly 25 % of the market, benefitting from early FDA approval and extensive clinical data. Aflibercept, a fusion protein that traps VEGF‑A, VEGF‑B and PlGF, accounts for about 30 % of sales, driven by its longer dosing interval and strong adoption in both AMD and DME. Bevacizumab, an off‑label oncology drug repurposed for ocular use, contributes approximately 20 % of volume, primarily because of its low acquisition cost despite lacking a dedicated ophthalmic label. Newer entrants such as Brolucizumab and Faricimab together represent near 15 % of the market, reflecting early‑stage uptake linked to extended durability claims. Biosimilar versions of ranibizumab and aflibercept are emerging, poised to capture the remaining 10 % as cost‑containing pressures intensify. This type‑based taxonomy clarifies competitive positioning and informs pricing, reimbursement, and R&D investment decisions across the Anti‑VEGF Therapies market.