Raise Series F · $275M · announced Sep 9, 2026 Company release ↗Source quote
Sep 9, 2026 · Company release ↗ “Encoded Therapeutics Raises $275 Million in Series F Financing to Advance ETX101 Through Pivotal Development and Accelerate its Precision Genetic Medicines Neurology Pipeline – Co led by GV and another healthcare fund”
Raises announced in these releases: $275M disclosed.
Trial start Phase 1/Phase 2: A Clinical Study to Evaluate the Safety and Efficacy of ETX101 in Infants and Children With SCN1A-Positive Dravet Syndrome source ↗
Trial start Phase 1/Phase 2: A Clinical Study to Evaluate the Safety and Efficacy of ETX101, an AAV9-Delivered Gene Therapy in Children With SCN1A-positive Dravet Syndrome source ↗
Trial start Phase 1/Phase 2: A Clinical Study to Evaluate the Safety and Efficacy of ETX101, an AAV9-Delivered Gene Therapy in Children With SCN1A-positive Dravet Syndrome (Australia Only) source ↗
Trial start —: Natural History Study of Infants and Children With Developmental and Epileptic Encephalopathies source ↗
Upcoming milestones
2028-01 (ESTIMATED) · Phase 1/Phase 2 · A Clinical Study to Evaluate the Safety and Efficacy of ETX101 in Infants and Children With SCN1A-Positive Dravet Syndrome · NCT05419492
2030-09 (ESTIMATED) · Phase 1/Phase 2 · A Clinical Study to Evaluate the Safety and Efficacy of ETX101, an AAV9-Delivered Gene Therapy in Children With SCN1A-positive Dravet Syndrome (Australia Only) · NCT06112275
2030-10 (ESTIMATED) · Phase 1/Phase 2 · A Clinical Study to Evaluate the Safety and Efficacy of ETX101, an AAV9-Delivered Gene Therapy in Children With SCN1A-positive Dravet Syndrome · NCT06283212
Estimated primary completion per ClinicalTrials.gov. Dates move.
A Clinical Study to Evaluate the Safety and Efficacy of ETX101, an AAV9-Delivered Gene Therapy in Children With SCN1A-positive Dravet Syndrome (Australia Only)
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