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in mil. unless spec.•
in mil. unless spec.•
in mil. unless spec.•
in mil. unless spec.•
in mil. unless spec.•
in mil. unless spec.Clinical Trial Results Show Extended Benefits for REGENXBIO Retinal Treatments
REGENXBIO Presents Positive Long-Term Data for Surabgene Lomparvovec in Wet AMD and Diabetic Retinopathy at American Society of Retina Specialists Annual Meeting
REGENXBIO Presents Positive Long-Term Data for Surabgene Lomparvovec in Wet AMD and Diabetic Retinopathy at American Society of Retina Specialists Annual Meeting
REGENXBIO Announces Pricing of Public Offering of Common Stock and Pre-funded Warrants
REGENXBIO Announces Proposed Public Offering of Common Stock
Kuehn Law Encourages Investors of Regenxbio, Inc. to Contact Law Firm
REGENXBIO Announces First Patient Dosed in Phase IIb/III NAAVIGATE Trial of Surabgene Lomparvovec in Diabetic Retinopathy; Company to Receive $100 Million Milestone
Regenxbio: 'Strong Buy' On FDA Course Reversal For NAVSUNLI And Potential AA DMD Filing
REGENXBIO Completes Dosing in Confirmatory Study of RGX-202, Marking Completion of Registrational Development Program and Supporting Planned BLA Submission in Q3 2026
Regenxbio Shares Rise on Plans to Resubmit Navsunli BLA for MPS II
Regenxbio Gains Fresh Chance As FDA Reconsiders Gene Therapy
REGENXBIO Announces Alignment with FDA on Path Forward for NAVSUNLI™ BLA Resubmission for Accelerated Approval; First Potential Gene Therapy for MPS II
FDA to reverse rejection of Regenxbio's rare-disease drug, WSJ reports
FDA Will Reverse Rejection of Third Rare-Disease Drug, Regenxbio Says
REGENXBIO Inc. (RGNX) Presents at RBC Capital Markets Global Healthcare Conference 2026 Transcript
REGENXBIO to Participate in Upcoming Investor Conferences
REGENXBIO Inc. (RGNX) Q1 2026 Earnings Call Transcript
REGENXBIO Advances Duchenne Gene Therapy Toward Accelerated Approval
Regenxbio (RGNX) Reports Q1 Loss, Lags Revenue Estimates
REGENXBIO Reports First Quarter 2026 Financial Results and Operational Highlights