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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Phenotype, Genotype & Biomarkers in ALS and Related DisordersCongenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Frontotemporal Lobar Degeneration, Nutritional and Metabolic Diseases, TDP-43 proteinopathy, amyotrophic lateral sclerosis, brain disorder, central nervous system disorder, central nervous system malformation, cognitive disorder, dementia, frontotemporal dementia, hereditary disease, hereditary motor and sensory neuropathy, hereditary spastic paraplegia, inherited neurodegenerative disorder, lateral sclerosis, metabolic disease, motor neuron disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathy, progressive muscular atrophy, proteostasis deficiencies, psychiatric disorder, spinal cord disorder, spinal muscular atrophyActive, not recruitingNot stated2026-06-15NCT02327845

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Research sitesCityCountryLinked trials
California Pacific Medical Center (CPMC)San FranciscoUnited States2
Cleveland ClinicClevelandUnited States558
Eberhard Karls University of TübingenTübingenGermany1
Kansas University Medical Center (KUMC)Kansas CityUnited States1
Stanford UniversityPalo AltoUnited States161
Twin Cities ALS Research ConsortiumMinneapolisUnited States1
University of California San Diego (UCSD)San DiegoUnited States1
University of Cape TownCape TownSouth Africa10
University of IowaIowa CityUnited States284
University of MiamiMiamiUnited States327
University of PennsylvaniaPhiladelphiaUnited States507
University of Texas Health Science Center San Antonio (UTHSCSA)San AntonioUnited States1
University of Texas Southwestern (UTSW)DallasUnited States2
University of Virginia (UVA)CharlottesvilleUnited States2
Wake Forest UniversityWinston-SalemUnited States22