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AGLE‑102, the lead candidate, is in a Phase 1/2 clinical trial for recessive dystrophic epidermolysis bullosa. Preclinical data show that AGLE‑102 can induce COL7 production and deliver COL7 protein to deficient fibroblasts, with potential benefits including reduced inflammation, enhanced healing, and improved tissue regeneration. Other programs are at preclinical stage targeting burns and graft vs. host disease. No published late-stage or commercial results yet.
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