Fondazione IRCCS Istituto Neurologico Carlo Besta | ClinicalTrials HQ

4 results · Page 1 of 1

Swipe the table sideways for more columns.

Trial	Conditions	Status	Phase	Updated	More info	NCT ID
A Study Comparing Niraparib With Temozolomide in Adult Participants With Newly-diagnosed, MGMT Unmethylated Glioblastoma	Neoplasms by Histologic Type, Neoplasms by Site, Neoplasms, Germ Cell and Embryonal, Neoplasms, Nerve Tissue, astrocytoma (excluding glioblastoma), brain disorder, central nervous system cancer, central nervous system disorder, epithelial neoplasm, glioblastoma, glioma, neoplasm, nervous system disorder, neuroepithelial neoplasm, primitive neuroectodermal tumor	Active, not recruiting	Phase 3	2026-07-01		NCT06388733
A Phase 1b/2 Study of IM-101 in Adult Participants With Generalized Myasthenia Gravis and Ocular Myasthenia Gravis	Neoplasms by Site, Paraneoplastic Syndromes, Nervous System, autoimmune disease, autoimmune disorder of the nervous system, immune system disorder, myasthenia gravis, neoplasm, nervous system disorder, neurodegenerative disease, neuromuscular disease, neuromuscular junction disease, paraneoplastic syndrome	Recruiting	Phase 1 / Phase 2	2026-02-11		NCT07250750
Autoimmune Dementia: Predictors of Neuronal Synaptic Antibodies in Patients With New-ONset Cognitive Impairment	Cognition Disorders, Cognitive Dysfunction, brain disorder, central nervous system disorder, cognitive disorder, dementia, nervous system disorder, psychiatric disorder	Recruiting	Not stated	2026-02-11		NCT06321588
Longitudinal Study of Ultra-rare Inherited Metabolic and Degenerative Neurological Diseases.	2-hydroxyglutaric aciduria, Alexander disease, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cysts, Digestive System Diseases, Disease Attributes, Hereditary Central Nervous System Demyelinating Diseases, Krabbe disease, Leukoencephalopathies, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Nervous System, Neurobehavioral Manifestations, Neurologic Manifestations, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, Pelizaeus-Merzbacher spectrum disorder, Peroxisomal Disorders, Rare Diseases, Sulfatidosis, Undiagnosed Diseases, Wilson disease, X-linked disease, adrenal gland disorder, adrenocortical insufficiency, adrenoleukodystrophy, basal ganglia disorder, bilateral striopallidodentate calcinosis, brain disorder, central nervous system disorder, cerebrotendinous xanthomatosis, demyelinating disease, endocrine system disorder, hereditary disease, inborn errors of metabolism, inborn metal metabolism disorder, inherited neurodegenerative disorder, intellectual disability, liver disorder, lysosomal lipid storage disorder, lysosomal storage disease, metabolic disease, metachromatic leukodystrophy, methylmalonic aciduria and homocystinuria, movement disorder, neoplasm, nervous system disorder, neurodegenerative disease, polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly, sphingolipidosis, xanthomatosis	Recruiting	Not stated	2024-11-19		NCT04880356