{"id":59398,"date":"2026-03-13T21:30:15","date_gmt":"2026-03-13T13:30:15","guid":{"rendered":"https:\/\/flcube.com\/?p=59398"},"modified":"2026-03-13T21:30:17","modified_gmt":"2026-03-13T13:30:17","slug":"everest-medicines-reports-positive-phase-iia-data-for-vis-101-dual-vegf-a-ang-2-inhibitor-shows-best-in-class-potential-in-wamd","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=59398","title":{"rendered":"Everest Medicines Reports Positive Phase IIa Data for VIS-101 \u2013 Dual VEGF-A\/Ang-2 Inhibitor Shows Best-in-Class Potential in wAMD"},"content":{"rendered":"\n<p><strong>Everest Medicines<\/strong> (<a href=\"https:\/\/www.google.com\/finance\/quote\/1952:HKG\">HKG: 1952<\/a>) announced <strong>positive topline results<\/strong> from its <strong>Phase IIa study of VIS-101<\/strong>, an investigational <strong>dual-functional biologic targeting VEGF-A and Ang-2<\/strong> for <strong>wet age-related macular degeneration (wAMD)<\/strong>. The data demonstrated <strong>rapid onset of action, potent and durable therapeutic response, and favorable safety<\/strong>, validating its potential as a <strong>&#8220;best-in-class&#8221; therapy<\/strong> for long-term durability in retinal vascular diseases.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-phase-iia-study-results\">Phase IIa Study Results<\/h2>\n\n\n\n<figure class=\"wp-block-table\"><table class=\"has-fixed-layout\"><thead><tr><th>Endpoint<\/th><th>VIS-101 Performance<\/th><th>Clinical Significance<\/th><\/tr><\/thead><tbody><tr><td><strong>Onset of Action<\/strong><\/td><td>Rapid<\/td><td>Immediate visual acuity benefits vs. standard of care<\/td><\/tr><tr><td><strong>Efficacy<\/strong><\/td><td>Potent and durable therapeutic response<\/td><td>Reduced injection frequency potential<\/td><\/tr><tr><td><strong>Safety\/Tolerability<\/strong><\/td><td>Favorable profile<\/td><td>Supports long-term chronic administration<\/td><\/tr><tr><td><strong>Best-in-Class Potential<\/strong><\/td><td>Validated<\/td><td>Dual-target mechanism vs. monotherapy alternatives<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><strong>Study Design:<\/strong> Phase IIa trial in wAMD patients; data supports expansion to diabetic macular edema (DME) and retinal vein occlusion (RVO)<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-product-profile-amp-mechanism\">Product Profile &amp; Mechanism<\/h2>\n\n\n\n<figure class=\"wp-block-table\"><table class=\"has-fixed-layout\"><thead><tr><th>Attribute<\/th><th>VIS-101 Specification<\/th><\/tr><\/thead><tbody><tr><td><strong>Mechanism<\/strong><\/td><td>Dual inhibition of <strong>VEGF-A<\/strong> (vascular permeability) + <strong>Ang-2<\/strong> (vascular stability)<\/td><\/tr><tr><td><strong>Format<\/strong><\/td><td>Novel biologic; investigational ophthalmic injectable<\/td><\/tr><tr><td><strong>Differentiation<\/strong><\/td><td>Addresses both pathological angiogenesis and vascular destabilization vs. anti-VEGF monotherapies<\/td><\/tr><tr><td><strong>Target Indications<\/strong><\/td><td>wAMD (lead), DME, RVO<\/td><\/tr><tr><td><strong>Expected Benefit<\/strong><\/td><td>More enduring therapeutic effect; reduced treatment burden<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><strong>Scientific Rationale:<\/strong> Ang-2 inhibition stabilizes vasculature compromised by VEGF-driven neovascularization, potentially extending durability beyond first-generation anti-VEGF agents (ranibizumab, aflibercept).<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-licensing-amp-geographic-rights\">Licensing &amp; Geographic Rights<\/h2>\n\n\n\n<figure class=\"wp-block-table\"><table class=\"has-fixed-layout\"><thead><tr><th>Element<\/th><th>Detail<\/th><\/tr><\/thead><tbody><tr><td><strong>Licensor<\/strong><\/td><td>Visara (subsidiary of NovaBridge Biosciences, NASDAQ: NBP)<\/td><\/tr><tr><td><strong>Licensee<\/strong><\/td><td>Everest Medicines (HKG: 1952)<\/td><\/tr><tr><td><strong>Territory<\/strong><\/td><td>Greater China, Singapore, South Korea, select Southeast Asian countries<\/td><\/tr><tr><td><strong>Rights<\/strong><\/td><td>Exclusive clinical development, manufacturing, commercialization<\/td><\/tr><tr><td><strong>Deal Date<\/strong><\/td><td>October 2025<\/td><\/tr><tr><td><strong>Deal Terms<\/strong><\/td><td>Not disclosed; typical milestone\/royalty structure for Phase II assets<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-market-context-amp-competitive-position\">Market Context &amp; Competitive Position<\/h2>\n\n\n\n<figure class=\"wp-block-table\"><table class=\"has-fixed-layout\"><thead><tr><th>Factor<\/th><th>Implication<\/th><\/tr><\/thead><tbody><tr><td><strong>wAMD Market Size<\/strong><\/td><td>Greater China <strong>$3+ billion<\/strong> annually; growing elderly population drives incidence<\/td><\/tr><tr><td><strong>Standard of Care<\/strong><\/td><td>Anti-VEGF monotherapies (aflibercept, ranibizumab biosimilars) require monthly\/bimonthly injections<\/td><\/tr><tr><td><strong>Durability Gap<\/strong><\/td><td>~40% of patients lose vision between injections; VIS-101 dual-target approach addresses unmet need for extended dosing intervals<\/td><\/tr><tr><td><strong>Competitive Landscape<\/strong><\/td><td>Faricimab (Roche) first dual Ang-2\/VEGF-A approved; VIS-101 positions as regional alternative with potentially differentiated profile<\/td><\/tr><tr><td><strong>Pipeline Synergy<\/strong><\/td><td>Everest&#8217;s ophthalmology portfolio includes other retinal assets; VIS-101 anchors wAMD franchise<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Development Pathway:<\/strong> Phase IIb\/III initiation expected 2026; potential for <strong>accelerated NMPA review<\/strong> given best-in-class data and unmet need in China<\/li>\n\n\n\n<li><strong>Commercial Outlook:<\/strong> Peak sales potential <strong>$500+ million in licensed territories<\/strong> assuming biannual dosing advantage and competitive pricing vs. faricimab<\/li>\n<\/ul>\n\n\n\n<p><strong>Forward\u2011Looking Statements<\/strong><br>This brief contains forward\u2011looking statements regarding clinical development timelines, regulatory pathways, and commercial potential for VIS-101. Actual results may differ due to Phase III trial outcomes, competitive dynamics with faricimab, and reimbursement negotiations in Greater China markets.<a href=\"https:\/\/flcube.com\/\">-Fineline Info &amp; Tech<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Everest Medicines (HKG: 1952) announced positive topline results from its Phase IIa study of VIS-101,&#8230;<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"googlesitekit_rrm_CAownpewDA:productID":"","_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":true,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2}},"categories":[7,10],"tags":[17,126,1164],"class_list":["post-59398","post","type-post","status-publish","format-standard","hentry","category-company","category-deals","tag-clinical-trial-results","tag-everest-medicines","tag-hkg-1952"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v23.6 (Yoast SEO v27.4) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>Everest Medicines Reports Positive Phase IIa Data for VIS-101 \u2013 Dual VEGF-A\/Ang-2 Inhibitor Shows Best-in-Class Potential in wAMD - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"Everest Medicines (HKG: 1952) announced positive topline results from its Phase IIa study of VIS-101, an investigational dual-functional biologic targeting VEGF-A and Ang-2 for wet age-related macular degeneration (wAMD). 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