SCN2A Encephalopathy

2

Review clinical trials related to SCN2A Encephalopathy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Clinical Trial of Elsunersen in Pediatric SCN2A-DEE to Assess Efficacy and Safety

A Multi-Center, Single-Arm Clinical Trial to Investigate the Efficacy and Safety of Elsunersen in Pediatric Participants with Early Onset SCN2A Developmental and Epileptic Encephalopathy

Participants needed: 40
Trial details
Phase: Phase 3Age: 1-18Biological sex: AllType: InterventionalSponsor: Praxis Precision MedicinesUpdated: May 27, 2026Locations: 10
Eligibility criteria

Has a documented Gain of Function SCN2A variant confirmed through genetic testin... [+2]

Has any clinically significant or known pathogenic genetic variant other than in... [+3]

Status: Recruiting

Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight

Simons Searchlight is an observational, online, international research program for families with rare genetic variants that cause neurodevelopmental disorders and may be associated with autism. Simons Searchlight collects medical, behavioral, learning, and developmental information from people who have these rare genetic changes. The goal of this study is to improve the clinical care and treatment for these people. Simons Searchlight partners with families to collect data and distribute it to qualified researchers.

Participants needed: 100,000
Trial details
Biological sex: AllType: ObservationalSponsor: Simons SearchlightUpdated: Jun 6, 2025Locations: 2
Eligibility criteria

Subjects of any age with a genetic condition on our eligible list along with the... [+3]