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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Phenylbutyrate for Monogenetic Developmental and Epileptic Encephalopathydevelopmental and epileptic encephalopathy, developmental and epileptic encephalopathy, 4Active, not recruitingEarly phase 12026-01-22NCT04937062
STXBP1 and SYNGAP1 Related Disorders Natural History StudyCongenital, Hereditary, and Neonatal Diseases and Abnormalities, developmental and epileptic encephalopathy, 4, hereditary diseaseRecruitingNot stated2025-10-29NCT06555965