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Developmental and epileptic encephalopathy, 33

MONDO:0014625

Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the EEF1A2 gene.

Also known as: DEE33, EEF1A2 early infantile epileptic encephalopathy, EEF1A2-Related Neurodevelopmental Disorder, EEF1A2-related neurodevelopmental disorder, EIEE33, developmental and epileptic encephalopathy 33, early infantile epileptic encephalopathy caused by mutation in EEF1A2, epileptic encephalopathy, early infantile, 33

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

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Broader categories

Disease (680) Epilepsy (438) Metabolic disease (233) Nervous system disorder (231) Hereditary disease (176) Neurodevelopmental disorder (147) Brain disorder (125) Central nervous system disorder (107) Inborn errors of metabolism (45) Developmental and epileptic encephalopathy (28)
Trials to join now! 5 Not yet finished but already full! 6 Completed 4 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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