REGENXBIO Reports Fourth Quarter and Full Year 2025 Financial Results and Operational Highlights
View original at finance.yahoo.comREGENXBIO Reports Fourth Quarter and Full Year 2025 Financial Results and Operational Highlights Late-stage gene therapy pipeline for rare and retinal diseases advancing toward key catalysts RGX-202 for Duchenne muscular dystrophy: New Phase I/II data at MDA, topline pivotal results expected early Q2 2026 Robust patien…
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All RGX-202 pivotal dose patients exceeded expected disease trajectory on NSAA, improving average of 7.4 points vs cTAP at 18 months
80% confidenceREGENXBIO is rapidly advancing late-stage pipeline with multiple near-term catalysts in 2026, driven by fully in-house capabilities, commercial-ready manufacturing, and global partners
80% confidenceREGENXBIO plans to request pre-BLA meeting in mid-2026 to align with FDA on BLA submission for RGX-202
80% confidenceThousands of patients have been treated with REGENXBIO's AAV platform, including those receiving Zolgensma
80% confidenceCash balance of $240.9M as of December 31, 2025 expected to fund operations into early 2027, excluding potential partner milestone payments and non-dilutive funding
80% confidenceREGENXBIO expects majority of confirmatory trial (n=30) enrolled at time of BLA submission
80% confidenceGlobal regulatory submissions for sura-vec wet AMD are expected in 2027
80% confidenceSura-vec is potentially the first-in-class treatment for wet AMD and diabetic retinopathy
80% confidenceAt two years post-treatment with sura-vec Dose Level 3 in ALTITUDE trial, no intraocular inflammation was observed (n=15), 50% achieved ≥2-step DRSS improvement, and ≥70% risk reduction in vision-threatening complications vs historical controls
80% confidenceREGENXBIO is working to address concerns in RGX-121 CRL with goal of resubmitting BLA
80% confidenceRGX-202 is designed to be a potential best-in-class gene therapy for Duchenne with unique C-Terminal domain inclusion for muscle protection
80% confidence
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