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News articleYahoo Finance· March 5, 2026

REGENXBIO Reports Fourth Quarter and Full Year 2025 Financial Results and Operational Highlights

View original at finance.yahoo.com
REGENXBIO 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% confidence
  • REGENXBIO 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% confidence
  • REGENXBIO plans to request pre-BLA meeting in mid-2026 to align with FDA on BLA submission for RGX-202

    80% confidence
  • Thousands of patients have been treated with REGENXBIO's AAV platform, including those receiving Zolgensma

    80% confidence
  • Cash 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% confidence
  • REGENXBIO expects majority of confirmatory trial (n=30) enrolled at time of BLA submission

    80% confidence
  • Global regulatory submissions for sura-vec wet AMD are expected in 2027

    80% confidence
  • Sura-vec is potentially the first-in-class treatment for wet AMD and diabetic retinopathy

    80% confidence
  • At 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% confidence
  • REGENXBIO is working to address concerns in RGX-121 CRL with goal of resubmitting BLA

    80% confidence
  • RGX-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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