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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
BMB-101 in Absence Epilepsy and DEECongenital, Hereditary, and Neonatal Diseases and Abnormalities, Epilepsies, Myoclonic, Epilepsy, Absence, Epilepsy, Generalized, Epileptic Syndromes, Lennox-Gastaut syndrome, brain disorder, central nervous system disorder, epilepsy, epilepsy with eyelid myoclonia, hereditary disease, nervous system disorderRecruitingPhase 22025-08-12NCT06401538