Evicenter
P&T meetings

Relutrigine

SCN2A- and SCN8A-related developmental and epileptic encephalopathies

Regulatory submission
NDA submitted in early 2026
Launch
Not announced
Last updated
72 sources

Product information and disease descriptionPlace of product in therapyApproaches to treatment

Place in treatment, anticipated use, and care setting

1 evidence topic · 5 sources

Summary

The studied use of relutrigine is as an investigational treatment for SCN2A- and SCN8A-related DEEs in participants already receiving antiseizure medications. In EMBOLD cohort 2, 34 participants exposed to relutrigine, representing 67%, were taking three to six ASMs at baseline. The manufacturer describes an oral or G/J-tube liquid formulation. Expanded-access requests require submission by the treating physician and are considered individually. These data describe study use and access arrangements, not an approved treatment position.