Overview

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)

Status:
Recruiting
Trial end date:
2029-12-01
Target enrollment:
0
Participant gender:
All
Summary
WAYFINDER is a Phase 1/2 study in Australia to evaluate the safety and efficacy of ETX101 in participants with SCN1A-positive Dravet syndrome aged 36 to <84 months (3 to <7 years). The study follows an open-label, dose-escalation design.
Phase:
Phase 1/Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Encoded Therapeutics
Criteria
Inclusion Criteria:

- Participant must have a predicted loss of function pathogenic or likely pathogenic
SCN1A variant.

- Participant must have experienced their first convulsive seizure between the ages of 3
and 15 months.

- Participant must have a clinical diagnosis of Dravet syndrome or the treating
clinician must have a high clinical suspicion of a diagnosis of Dravet syndrome.

- Participant is receiving at least one prophylactic antiseizure medication.

Exclusion Criteria:

- Participant has another genetic mutation or clinical comorbidity which could
potentially confound the typical Dravet phenotype.

- Participant has a known central nervous system structural and/or vascular abnormality
(indicated by an MRI or CT scan of the brain).

- Participant has an abnormality that may interfere with CSF distribution and/or has an
existing ventriculoperitoneal shunt.

- Participant is currently taking or has taken antiseizure medications (ASMs) at a
therapeutic dose that are contraindicated in Dravet syndrome, including sodium channel
blockers.

- Participant has experienced seizure freedom for a period of 4 consecutive weeks within
the 6-month period prior to informed consent.

- Participant has previously received gene or cell therapy.

- Participant is currently enrolled in a clinical trial or receiving an investigational
therapy.

- Participant has clinically significant underlying liver disease.