Lennox-Gastaut syndrome

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Information
Disease name
Lennox-Gastaut syndrome
Disease ID
DOID:0050561
Description
"A childhood electroclinical syndrome that is characterized by frequent seizures and intellectual disability that present in early childhood." [url:https\://ghr.nlm.nih.gov/condition/lennox-gastaut-syndrome]
Disease area statistics
Chromosome band
Gene symbol Chromosome Start Stop The number of variant
DNM1 9 128,203,417 128,255,239 4
CIZ1 9 128,166,066 128,191,939 4
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT05626634 Active, not recruiting Phase 2 Open-label, Long-term Safety Study of LP352 in Subjects With Developmental and Epileptic Encephalopathy November 8, 2022 October 2024
NCT00004776 Completed Phase 3 Phase III Randomized, Double-Blind, Placebo-Controlled Study of Oral Topiramate for Lennox-Gastaut Syndrome November 1993
NCT00552045 Completed Epilepsy Phenome/Genome Project November 2007 October 2018
NCT01146951 Completed Phase 3 A Placebo-Controlled, Double-Blind Comparative Study of E2080 in Lennox-Gastaut Syndrome Patients (Study E2080-J081-304) June 2010 August 2011
NCT01151540 Completed Phase 3 A Long Term Extension Study of E2080 in Lennox-Gastaut Patients November 2010 August 2013
NCT01160770 Completed Phase 3 Safety and Effectiveness of Open-Label Clobazam in Subjects With Lennox-Gastaut Syndrome December 2005 February 2012
NCT01405053 Completed Phase 3 Study of Rufinamide in Pediatric Subjects 1 to Less Than 4 Years of Age With Lennox-Gastaut Syndrome Inadequately Controlled With Other Anti-epileptic Drugs June 16, 2011 November 2, 2015
NCT01991041 Completed European Registry of Anti-Epileptic Drug Use in Patients With Lennox-Gastaut Syndrome (LGS) June 2008 November 2015
NCT02175173 Completed Post-marketing Surveillance of Long-term Administration of Inovelon Tablets in Patients With Lennox-Gastaut Syndrome June 13, 2013 November 2, 2022
NCT00004729 Completed N/A Ketogenic Diet for Child Epilepsy and Seizure Control July 1997
NCT02224690 Completed Phase 3 A Study to Investigate the Efficacy and Safety of Cannabidiol (GWP42003-P; CBD) as Adjunctive Treatment for Seizures Associated With Lennox-Gastaut Syndrome in Children and Adults April 28, 2015 March 18, 2016
NCT02224573 Completed Phase 3 An Open Label Extension Study of Cannabidiol (GWP42003-P) in Children and Adults With Dravet or Lennox-Gastaut Syndromes June 11, 2015 September 24, 2020
NCT02731300 Completed Phase 4 Transcranial Direct Current Stimulation, Treatment of Childhood Drug-Resistant Lennox-Gastaut Syndrome, A Pilot Study August 2010 December 2013
NCT03650452 Completed Phase 2 A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy, Safety, and Tolerability of TAK-935 (OV935) as an Adjunctive Therapy in Pediatric Participants With Developmental and/or Epileptic Encephalopathies August 8, 2018 July 20, 2020
NCT02815540 Terminated Phase 1/Phase 2 The Effects of Cannabidiol (CBD) on Electrical and Autonomic Cardiac Function in Children With Severe Epilepsy February 16, 2017 December 1, 2018
NCT02632149 Unknown status Early Phase 1 Trial to Assess Vagus Nerve Stimulation Therapy in Children With Lennox-Gastaut Syndrome October 2016
NCT04133480 Withdrawn Phase 4 Investigation of Cognitive Outcomes With Cannabidiol Oral Solution October 2020 December 2021
NCT03254680 Withdrawn N/A Turmeric as Treatment in Epilepsy March 2018 November 2018
NCT01370486 Withdrawn Phase 4 Melatonin Versus Placebo in the Lennox-Gastaut Syndrome: Neurophysiological and Neuropsychological Effects August 2011 January 2012
NCT02318537 Withdrawn Phase 3 Cannabidiol Oral Solution as an Adjunctive Therapy for Treatment of Participants With Inadequately Controlled Lennox-Gastaut Syndrome December 30, 2017 June 30, 2018
Disase is a (Disease Ontology)
DOID:0050704
Cross Reference ID (Disease Ontology)
GARD:9912
Cross Reference ID (Disease Ontology)
MESH:D065768
Cross Reference ID (Disease Ontology)
MIM:606369
Cross Reference ID (Disease Ontology)
ORDO:2382
Exact Synonym (Disease Ontology)
Lennox syndrome
OrphaNumber from OrphaNet (Orphanet)
2382