Hemimegalencephaly: Clinical Trials

3 trials for Hemimegalencephaly, newest first

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2 recruiting, 1 withdrawn. 1 Not applicable, 1 Phase 1, 1 Phase 2.

By phase and status

PhaseTrialsStatus
Not applicable1Withdrawn 1
Phase 11Recruiting 1
Phase 21Recruiting 1

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

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
Safety, Tolerability, and Pharmacokinetics of SVG103 (Paxalisib) in Focal Cortical Dysplasia Type II (FCD-II), Tuberous Sclerosis Complex (TSC) or Hemimegalencephaly (HME)
SVG103 - Focal Cortical Dysplasia, Tuberous Sclerosis Complex (TSC)
Phase 1 / Phase 2RecruitingSovargen122026-07-142026-08-10
Use of a Tonometer to Identify Epileptogenic Lesions During Pediatric Epilepsy Surgery
Intra-operative brain tonometry - Epilepsy, Focal Cortical Dysplasia
Not applicableWithdrawnUniversity of California, Los Angeles2018-07-162023-10-10
Genetic and Electrophysiologic Study in Focal Drug-resistant Epilepsies
Sampling of blood, frozen resected tissues, and cerebrospinal fluid (CSF) - Drug-resistant Focal Epilepsies in Pediatric Population
RecruitingFondation Ophtalmologique Adolphe de Rothschild4502015-12-172026-04-17

Narrower conditions

Focal Cortical Dysplasia (3)  ·  Tuberous Sclerosis (3)  ·  Encephalitis (2)  ·  Brain Neoplasms (1)  ·  Epilepsies, Partial (1)  ·  Epilepsy (1)  ·  Gliosis (1)  ·  Hypothalamic hamartomas (1)  ·  Polymicrogyria (1)  ·  Stroke (1)  ·  Sturge-Weber Syndrome (1)

Broader conditions

Congenital Abnormalities (3)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (3)  ·  Craniofacial Abnormalities (3)  ·  Genetic Diseases, Inborn (3)  ·  Hamartoma (3)  ·  Heredodegenerative Disorders, Nervous System (3)  ·  Malformations of Cortical Development (3)  ·  Malformations of Cortical Development, Group I (3)  ·  Megalencephaly (3)  ·  Musculoskeletal Abnormalities (3)  ·  Musculoskeletal Diseases (3)  ·  Neoplasms (3)  ·  Neoplasms, Multiple Primary (3)  ·  Neoplastic Syndromes, Hereditary (3)  ·  Nervous System Diseases (3)

Sponsors

Fondation Ophtalmologique Adolphe de Rothschild (1)  ·  Sovargen (1)  ·  University of California, Los Angeles (1)

Countries

Australia (1)  ·  Canada (1)  ·  France (1)  ·  United States (1)

Top investigators

Aria Fallah, MD (1)

Results publications

PMID 31444548, PMID 33407896, PMID 33434304, PMID 33834539, PMID 36307217, PMID 37324239, PMID 38710875, PMID 39460693, PMID 40307383