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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
PrProfile: A Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ION717Infections, central nervous system disorder, central nervous system infectious disorder, nervous system disorder, neurodegenerative disease, prion diseaseActive, not recruitingPhase 1 / Phase 22026-09-18NCT06153966
A Study to Investigate LP352 in Children and Adults With Developmental and Epileptic Encephalopathy (DEE)Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Epilepsies, Myoclonic, Epilepsy, Generalized, Epileptic Syndromes, Lennox-Gastaut syndrome, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, brain disorder, central nervous system disorder, developmental and epileptic encephalopathy, epilepsy, hereditary disease, nervous system disorder, neurodevelopmental disorder, psychiatric disorder, visual epilepsyEnrolling by invitationPhase 32026-09-15NCT06908226
A Study to Investigate LP352 in Children and Adults With Developmental and Epileptic Encephalopathies (DEE)Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Epileptic Syndromes, Lennox-Gastaut syndrome, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, brain disorder, central nervous system disorder, developmental and epileptic encephalopathy, epilepsy, hereditary disease, nervous system disorder, neurodevelopmental disorder, psychiatric disorder, visual epilepsyActive, not recruitingPhase 32026-09-15NCT06719141
Neurovascular Product Surveillance RegistryAneurysm, brain aneurysm, brain disorder, cardiovascular disorder, central nervous system disorder, cerebrovascular disorder, intracranial arterial disease, ischemic stroke, nervous system disorder, stroke disorder, vascular disorderRecruitingNot stated2026-09-15NCT02988128
A Study of Eptinezumab in Pediatric Participants With Episodic MigraineEpisodic MigraineRecruitingPhase 32026-09-09NCT05897320
HDClarity: a Multi-site Cerebrospinal Fluid Collection Initiative to Facilitate Therapeutic Development for Huntington's DiseaseCognition Disorders, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyskinesias, Huntington disease, basal ganglia disorder, brain disorder, central nervous system disorder, choreatic disease, cognitive disorder, dementia, hereditary disease, inherited neurodegenerative disorder, movement disorder, nervous system disorder, neurodegenerative disease, psychiatric disorderRecruitingNot stated2026-04-27NCT02855476