Not applicableStudy completedNCT05161494What this trial is testingGait in Rare DiseasesWho this might be right forTuberous SclerosisSTXBP1 Encephalopathy With Epilepsy Universiteit Antwerpen 41
Testing effectiveness (Phase 2)Ended earlyNCT06983158What this trial is testingA Clinical Trial of CAP-002 Gene Therapy in Pediatric Patients With Syntaxin-Binding Protein 1 (STXBP1) EncephalopathyWho this might be right forDevelopmental and Epileptic Encephalopathy Capsida Biotherapeutics, Inc. 1
Not applicableNot Yet RecruitingNCT06356233What this trial is testingPhenotyping and Identification of Biological Markers in STXBP1 EncephalopathyWho this might be right forSTXBP1 Encephalopathy With Epilepsy Fundación Iniciativa para las Neurociencias (FINCE) 10
Not applicableLooking for participantsNCT06625112What this trial is testingA Multicentric European Study to Promote Clinical Trial Readiness for STXBP1-related DisordersWho this might be right forSTXBP1 Encephalopathy With Epilepsy European STXBP1 Consortium 120
Not applicableLooking for participantsNCT01238250What this trial is testingOnline Study of People Who Have Genetic Changes and Features of Autism: Simons SearchlightWho this might be right for16P11.2 Deletion Syndrome16p11.2 Duplications1Q21.1 Deletion+184 more Simons Searchlight 100,000
Post-approval studies (Phase 4)UnknownNCT05232630What this trial is testingFenfluramine for the Treatment of Different Types of Developmental and Epileptic Encephalopathies: a Pilot Trial Exploring Epileptic and Non-epileptic OutcomesWho this might be right forRefractory EpilepsySYNGAP1 EncephalopathySTXBP1 Encephalopathy With Epilepsy+3 more Hospital Ruber Internacional 20
Not applicableWithdrawnNCT05462054What this trial is testingNatural History Study in Pediatric Patients with STXBP1 Encephalopathy with EpilepsyWho this might be right forSTXBP1 Encephalopathy with Epilepsy Capsida Biotherapeutics, Inc.
Not applicableLooking for participantsNCT06555965What this trial is testingSTXBP1 and SYNGAP1 Related Disorders Natural History StudyWho this might be right forGenetic DiseaseSTXBP1 Encephalopathy With EpilepsySYNGAP1-Related Intellectual Disability Children's Hospital of Philadelphia 600
Very early researchActive Not RecruitingNCT04937062What this trial is testingPhenylbutyrate for Monogenetic Developmental and Epileptic EncephalopathyWho this might be right forSTXBP1 Encephalopathy With Epilepsy, SLC6A1 Neurodevelopmental DisorderDevelopmental and Epileptic Encephalopathy Weill Medical College of Cornell University 50