Natural History Study of Infants and Children With Developmental and Epileptic Encephalopathies

Expanded Access Use of Stiripentol in Dravet Syndrome or Sodium Channel Mutation Epileptic Encephalopathies

NCT02239276 ·Status: NO_LONGER_AVAILABLE

Extension Study to Evaluate How Safe and Tolerable NBI-921352 is as an Adjunctive Therapy for Participants With SCN8A-DEE

NCT05226780 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2

European Non-interventional Study on Refractory Epilepsy With Developmental Delay

NCT04398667 ·Status: TERMINATED

Cardiac Arrhythmias in Dravet Syndrome

NCT02415686 ·Status: COMPLETED

Extended Access Program With Lorcaserin For The Treatment of Dravet Syndrome and Other Refractory Epilepsies

NCT04457687 ·Status: AVAILABLE

A Study of Divalproex Sodium in Children With ASD and Epileptiform EEG

NCT01170325 ·Status: WITHDRAWN ·Phase: PHASE2

BMB-101 in Absence Epilepsy and DEE

NCT06401538 ·Status: RECRUITING ·Phase: PHASE2

Novel Epidermal Recording and Detection of Seizures

NCT02451618 ·Status: TERMINATED

Genotype, Phenotype, and Disease Progression of Developmental Epileptic Encephalopathy With Onset Before 2 Years of Age

NCT06278428 ·Status: RECRUITING

A Study to Gather Information About Overall Occurrence and New Cases of Dravet and Lennox-Gastaut Syndromes in Children, Teenagers and Adults in Spain

NCT05982717 ·Status: COMPLETED

Pathophysiology Based Therapy of Early Onset Epileptic Encephalopathies

NCT02968966 ·Status: WITHDRAWN ·Phase: PHASE2

A Clinical Trial of PRAX-222 in Pediatric Participants With Early Onset SCN2A Developmental and Epileptic Encephalopathy

NCT05737784 ·Status: RECRUITING ·Phase: PHASE1/PHASE2

Extension Study to Evaluate NBI-827104 in Pediatric Participants With Epileptic Encephalopathy With Continuous Spike-and-Wave During Sleep

NCT05301894 ·Status: TERMINATED ·Phase: PHASE2

A Clinical Trial of PRAX-562 in Subjects With Developmental and Epileptic Encephalopathies (DEE)

NCT05818553 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2/PHASE3

Preventing Epilepsy Using Vigabatrin In Infants With Tuberous Sclerosis Complex

NCT02849457 ·Status: COMPLETED ·Phase: PHASE2

A Cohort Study on the Prognosis of Neonatal KCNQ2 Gene-associated Epileptic Encephalopathy

NCT03934268 ·Status: UNKNOWN

A Phase 3, Placebo-Controlled Study to Investigate LP352 in Children and Adults With Dravet Syndrome (DS)

NCT06660394 ·Status: RECRUITING ·Phase: PHASE3

A Natural History Study of Participants With Potassium Sodium-Activated Channel Subfamily T Member 1 (KCNT1)-Related Epilepsy

NCT04924153 ·Status: COMPLETED

Phenylbutyrate for Monogenetic Developmental and Epileptic Encephalopathy

NCT04937062 ·Status: ACTIVE_NOT_RECRUITING ·Phase: EARLY_PHASE1

A Study of the Effects of JNJ-26489112 on the Photic Induced Paroxysmal Electroencephalogram (EEG) Response in Patients With Photosensitive Epilepsy

NCT00579384 ·Status: COMPLETED ·Phase: PHASE2

Study of Antiepileptic Drug Effects on Child Development

NCT00353886 ·Status: COMPLETED

CNKSR2 Natural History Study

NCT06500260 ·Status: RECRUITING

LEONIDaS Caregivers Study

NCT05140122 ·Status: WITHDRAWN

Fenfluramine for Adult Dravet Patients

NCT05560282 ·Status: TERMINATED ·Phase: PHASE3

Childhood Absence Epilepsy Rx PK-PD-Pharmacogenetics Study

NCT00088452 ·Status: COMPLETED ·Phase: PHASE3