Dravet Syndrome: Clinical Trials

62 trials for Dravet Syndrome, newest first

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

22 completed, 9 active not recruiting, 9 recruiting, 5 terminated. 17 Phase 3, 13 Phase 2, 10 Phase 1, 4 Not applicable, 2 Phase 4.

By phase and status

PhaseTrialsStatus
Phase 317Completed 8, Terminated 3, Active not recruiting 2, Withdrawn 2, Recruiting 1, Unknown 1
Phase 213Completed 6, Active not recruiting 3, Recruiting 3, Terminated 1
Phase 110Completed 5, Active not recruiting 2, Recruiting 2, Terminated 1
Not applicable4Active not recruiting 1, Recruiting 1, Unknown 1, Withdrawn 1
Phase 42Active not recruiting 1, Recruiting 1

Follow Dravet Syndrome: new trials by email Literature Review of Dravet Syndrome trials Research Report on Dravet Syndrome

Trials newest first · largest first

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
ASCEND: Safety and Tolerability of ION337 for the Treatment of Dravet Syndrome
ION337 - Dravet Syndrome
Phase 1 / Phase 2RecruitingIonis Pharmaceuticals, Inc.322026-05-212026-09-03
A PET-MRI Study of Serotoninergic Brainstem Pathway in Patients With Dravet Syndrome
[18F]MPPF PET-MRI - Epilepsy, Dravet Syndrome
Not applicableRecruitingHospices Civils de Lyon302026-05-042026-05-08
The FINTEPLA as an Anti-SUDEP Therapy in Dravet Syndrome Project
Fenfluramine treatment (Fintepla), Hypercapnia Challenge using the device (RespirAct) - Dravet Syndrome
Phase 4RecruitingThe University of Texas Health Science Center, Houston252026-04-272026-07-15
Multicentre Real-life Follow-up Study of Rare Epileptic Syndromes in Children and Adolescents
Epilepsy, West Syndrome
RecruitingAssistance Publique - Hôpitaux de Paris10002025-12-112026-02-24
Longitudinal Study of Phenotypic and Developmental Severity in Patients With Dravet Syndrome With SCN1A Gene Mutation
Dravet Syndrome
RecruitingAssistance Publique - Hôpitaux de Paris502025-09-152026-02-03
A Double-blind Study Evaluating the Efficacy, Safety, and Tolerability of Zorevunersen in Patients With Dravet Syndrome
zorevunersen, Sham Comparator - Dravet Syndrome
Phase 3Active not recruitingStoke Therapeutics, Inc1702025-06-042026-10-20
Bioavailability of Stiripentol After Single Oral Dose of Capsule vs Suspension in Healthy Subjects (STILIQ)
Stiripentol capsule (Diacomit®), Stiripentol oral suspension (Diacomit®) - Dravet Syndrome, Epilepsy
Phase 1CompletedBiocodex242025-06-012025-09-16
Epidyolex® in Lennox Gastaut, Dravet Syndrome and Tuberous Sclerosis Complex: an Observational Study in ITALY
Epidiolex 100 mg/mL Oral Solution - Lennox Gastaut Syndrome, Dravet Syndrome
Active not recruitingJazz Pharmaceuticals1112025-02-242026-06-03
BMB-101 in Absence Epilepsy and DEE
BMB-101 - Absence Epilepsy, Jeavons Syndrome
Phase 2RecruitingBright Minds Biosciences Pty Ltd202024-12-052025-08-12
A Phase 3, Placebo-Controlled Study to Investigate LP352 in Children and Adults With Dravet Syndrome (DS)
LP352, Placebo - Dravet Syndrome
Phase 3Active not recruitingLongboard Pharmaceuticals962024-09-252026-09-17
A Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Fenfluramine (Hydrochloride) in Infants 1 Year to Less Than 2 Years of Age With Dravet Syndrome
fenfluramine - Dravet Syndrome
Phase 3CompletedUCB BIOSCIENCES, Inc.252024-05-212026-09-17
A Clinical Study to Evaluate the Safety and Efficacy of ETX101 in Infants and Children With SCN1A-Positive Dravet Syndrome
ETX101 - Dravet Syndrome
Phase 1 / Phase 2RecruitingEncoded Therapeutics1132024-05-142026-10-23
A Clinical Study to Evaluate the Safety and Efficacy of ETX101, an AAV9-Delivered Gene Therapy in Children With SCN1A-positive Dravet Syndrome
ETX101 - Dravet Syndrome
Phase 1 / Phase 2Active not recruitingEncoded Therapeutics52024-05-092026-06-08
A Clinical Study to Evaluate the Safety and Efficacy of ETX101, an AAV9-Delivered Gene Therapy in Children With SCN1A-positive Dravet Syndrome (Australia Only)
ETX101 - Dravet Syndrome
Phase 1 / Phase 2Active not recruitingEncoded Therapeutics42024-02-282025-11-14
SCN1A Horizons A Natural History Study of SCN1A-related Epilepsies in the United Kingdom
SCN1A, Dravet Syndrome
UnknownNHS Greater Glasgow and Clyde4002023-11-202024-07-16
LEONIDaS Caregivers Study
Multiple - Dravet Syndrome, Depression
WithdrawnUniversity of Oxford2023-10-262023-12-14
EXploring novEl Molecular Determinants of DRAvet Syndrome Phenotype Heterogeneity
skin punch biopsy - Dravet Syndrome
Not applicableUnknownFondazione Policlinico Universitario Agostino Gemelli IRCCS162023-07-062024-04-17
Fenfluramine for Adult Dravet Patients
Fenfluramine - Dravet Syndrome, Dravet Syndrome, Intractable
Phase 3TerminatedUniversity Health Network, Toronto72023-01-112026-05-05
Open-label, Long-term Safety Study of LP352 in Subjects With Developmental and Epileptic Encephalopathy
LP352, bexicaserin - Developmental and Epileptic Encephalopathy, Dravet Syndrome
Phase 2CompletedLongboard Pharmaceuticals412022-11-082025-12-03
Neurodevelopmental Impact of Epilepsy on Autonomic Function in Dravet Syndrome
Video-electroencephalography, Blood Samples - Dravet Syndrome, Epilepsy
Not applicableActive not recruitingHospices Civils de Lyon922022-10-142026-01-14

Showing 20 of 62. Sign in to see all of them.

Narrower conditions

Epilepsies, Myoclonic (62)  ·  Epilepsy (24)  ·  Lennox Gastaut Syndrome (14)  ·  Seizures (10)  ·  Tuberous Sclerosis (7)  ·  Brain Diseases (5)  ·  CDKL5 deficiency disorder (4)  ·  Anemia, Sickle Cell (2)  ·  Cystic Fibrosis (2)  ·  Diabetes Mellitus (2)  ·  Generalized Epilepsy With Febrile Seizures Plus, Type 2 (2)  ·  Spasms, Infantile (2)  ·  Sudden Unexpected Death in Epilepsy (2)  ·  beta-Thalassemia (2)  ·  3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (1)

Broader conditions

Epilepsy, Generalized (62)  ·  Epileptic Syndromes (62)  ·  Central Nervous System Diseases (61)  ·  Nervous System Diseases (61)  ·  Brain Diseases (57)  ·  Epilepsy (38)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (16)  ·  Genetic Diseases, Inborn (16)  ·  Pathological Conditions, Signs and Symptoms (16)  ·  Neurologic Manifestations (12)  ·  Signs and Symptoms (11)  ·  Neurodegenerative Diseases (9)  ·  Congenital Abnormalities (8)  ·  Heredodegenerative Disorders, Nervous System (8)  ·  Neoplasms (8)

Interventions

Cannabidiol (10)  ·  Fenfluramine (10)  ·  stiripentol (5)  ·  Clobazam (2)  ·  Blood Specimen Collection (1)  ·  Curcumin (1)  ·  Electroencephalography (1)  ·  Retrospective Studies (1)  ·  Solutions (1)  ·  Suspensions (1)  ·  Transcranial Magnetic Stimulation (1)  ·  Verapamil (1)

Sponsors

Jazz Pharmaceuticals (5)  ·  Zogenix International Limited, Inc., a subsidiary of Zogenix, Inc. (5)  ·  Encoded Therapeutics (4)  ·  Longboard Pharmaceuticals (4)  ·  Gillette Children's Specialty Healthcare (3)  ·  Stoke Therapeutics, Inc (3)  ·  Assistance Publique - Hôpitaux de Paris (2)  ·  Biocodex (2)  ·  Cook Children's Health Care System (2)  ·  Epygenix (2)  ·  Fondazione Policlinico Universitario Agostino Gemelli IRCCS (2)  ·  H. Lundbeck A/S (2)  ·  Hospices Civils de Lyon (2)  ·  University of Colorado, Denver (2)  ·  Zogenix, Inc. (2)

Countries

United States (41)  ·  United Kingdom (14)  ·  Australia (13)  ·  France (13)  ·  Spain (10)  ·  Canada (9)  ·  Italy (9)  ·  Germany (8)  ·  Belgium (7)  ·  Poland (5)  ·  Denmark (4)  ·  Japan (4)  ·  Mexico (4)  ·  Netherlands (4)  ·  China (3)

Top investigators

Salvador Rico, M.D., Ph.D (3)  ·  Ann Dandurand, MD (2)  ·  Beverly S Wical, MD (2)  ·  Dennis J Dlugos, MD (2)  ·  Alexander Rotenberg, MD, PhD (1)  ·  Amit Ray, MD (1)  ·  Andreas Brunklaus, MD PhD (1)  ·  Ann Hallemans, PhD (1)  ·  Catherine Harmer, PhD (1)  ·  Christos Papadelis, PhD (1)  ·  Curt Scharfe, MD, PhD (1)  ·  Domenica Immacolata Battaglia (1)

Results publications

PMID 34768178, PMID 33540241, PMID 34265088, PMID 41780062, PMID 28538134, PMID 29768152, PMID 30644536, PMID 30940509, PMID 31315600, PMID 31582194, PMID 31790543, PMID 31862249, PMID 32119035, PMID 33230827, PMID 33445140, PMID 33445141, PMID 34287833, PMID 34406656, PMID 34666230, PMID 34676542, PMID 35142618, PMID 35841234, PMID 37543865, PMID 40072476

NIH funding

2014 (4), 2016 (1), 2018 (1), 2019 (1)