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RGNX

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  • FDA placed RGX-121 on clinical hold following spinal MRI findings in MPS IIAug 24, 2026

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  • REGENXBIO presents positive three-year durability data for surabgene lomparvovec in diabetic retinopathySep 25, 2026
  • REGENXBIO presents positive long-term data for Surabgene Lomparvovec in wet AMD and diabetic retinopathyJul 19, 2026
  • REGENXBIO dosed the first patient in the Phase IIb/III NAAVIGATE trial and became eligible for a $100 million milestone paymentJun 29, 2026
  • REGENXBIO completed dosing in the confirmatory RGX-202 study, supporting a planned BLA submission in Q3 2026Jun 24, 2026
  • REGENXBIO aligned with FDA on the path toward resubmitting the NAVSUNLI BLA for accelerated approval in MPS IIJun 22, 2026

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