SGT-501 is a novel gene therapy for rare, life-threatening, genetic arrhythmogenic disease with no approved therapies SGT-501 has received Orphan Drug Designation and Rare Pediatric Disease Designation from the FDA Solid expects to initiate Phase 1b clinical trial of SGT-501 in the fourth quarter of 2025 Expands Solid’s clinical pipeline to include first cardiac indication with urgent unmet medical need CHARLESTOWN, Mass.,... Read More