The goal of this trial is to learn about the effect of PRAX-222 in pediatric participants with early onset SCN2A developmental and epileptic encephalopathy (DEE), aged 2 to 18 years.
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Number of participants with treatment-emergent adverse events (Preliminary Safety, Dose Escalation)
Timeframe: Screening (-8 weeks) through up to 92 weeks
Seizure frequency (Confirmatory Phase)
Timeframe: 36 to 40 weeks