Regenxbio Touts Positive Biomarker Data From Duchenne Muscular Dystrophy Gene Therapy Trial
Results were presented at the 2025
At dosing, microdystrophin expression was 122.3% higher in a patient age three compared to the control.
In a patient age seven, RGX-202 microdystrophin expression was 31.5% higher than in the control.
In all patients, RGX-202 was appropriately localized to the sarcolemma, demonstrating the differentiated construct with the CT-Domain is appropriately targeting the muscle.
RGX-202 microdystrophin expression results in ambulatory patients age eight and above are the highest reported microdystrophin levels across approved or investigational gene therapies.
To support a Biologics License Application (BLA) using the accelerated approval pathway, the primary endpoint in the pivotal phase of AFFINITY DUCHENNE is the proportion of participants whose RGX-202 microdystrophin expression is ≥10% at Week 12.
RGX-202 also demonstrates the highest reported vector genome copies (4.9-55.4) measured by qPCR across approved or investigational gene therapies.
As of Feb. 21, 2025, RGX-202 was well tolerated, with no serious adverse events or AEs of special interest. Common drug-related AEs included nausea, vomiting and fatigue. All were resolved and typically anticipated with gene therapy administration.
Phase 3 portion of the AFFINITY DUCHENNE trial is enrolling ambulatory patients (who can walk) aged one and above, on track for BLA submission in mid-2026.
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