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Non-neonatal early infantile epileptic encephalopathy

MONDO:0100107

Non-neonatal early-onset epileptic encephalopathy is a form an of age-related epileptic encephalopathies, characterized by the onset of seizures later than the first 4 weeks of life but within the first three months. Seizures can be generalized or lateralized, independent of the sleep cycle and can occur multiple times per day, leading to psychomotor impairment and death.

39 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Epilepsy (398) Nervous system disorder (217) Hereditary disease (172) Neurodevelopmental disorder (125) Brain disorder (110) Central nervous system disorder (97) Developmental and epileptic encephalopathy (26) Human disease (14) Hereditary neurological disease (5)
Trials to join now! 18 Not yet recruiting 6 Not yet finished but already full! 7 Completed 7 Terminated 1
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  • New drug shows promise for Tough-to-Treat seizures in kids

    Disease control Terminated

    This study looked at the long-term safety of soticlestat, an experimental drug, in children and adults with severe forms of epilepsy like Dravet syndrome and Lennox-Gastaut syndrome. Participants took soticlestat twice a day along with their usual seizure medicines. The study was…

    Phase: PHASE2 • Sponsor: Takeda • Aim: Disease control

    Last updated Jun 27, 2026 11:03 UTC

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