Stopped: Business decision
The primary objective for this study is to evaluate the long-term safety and tolerability of NBI-827104 in pediatric participants with epileptic encephalopathy with continuous spike-and-wave during sleep (EECSWS).
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The Number of Participants With Serious Treatment-emergent Adverse Events (TEAEs)
Timeframe: Up to 884 days of treatment and 4-week safety follow-up (mean duration of exposure was 649.7 days)