Phenotype, Genotype and Biomarkers 2
NCT04875416 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 217
Last updated 2026-03-23
Summary
The purpose of this study is to learn more about amyotrophic lateral sclerosis (ALS) and other related neurodegenerative diseases, including frontotemporal dementia (FTD), primary lateral sclerosis (PLS), hereditary spastic paraplegia (HSP), progressive muscular atrophy (PMA) and multisystem proteinopathy (MSP). More precisely, the investigator wants to identify the links that exist between the disease phenotype (phenotype refers to observable signs and symptoms) and the disease genotype (genotype refers to your genetic information). The investigator also wants to identify biomarkers of ALS and related diseases.
Conditions
- Amyotrophic Lateral Sclerosis
- Hereditary Spastic Paraplegia
- Primary Lateral Sclerosis
- Progressive Muscular Atrophy
- Frontotemporal Dementia
Sponsors & Collaborators
-
National Institutes of Health (NIH)
collaborator NIH -
National Institute of Neurological Disorders and Stroke (NINDS)
collaborator NIH -
University of Miami
lead OTHER
Principal Investigators
-
Michael Benatar, MD, PhD · University of Miami
Eligibility
- Min Age
- 7 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2021-01-08
- Primary Completion
- 2026-09-30
- Completion
- 2028-08-31
Countries
- United States
- South Africa
Study Locations
More Related Trials
-
Genetic Study of Familial and Sporadic ALS/Motor Neuron Disease, Miyoshi Myopathy and Other Neuromuscular Disorders
NCT01459302 ·Status: WITHDRAWN
-
Nuclear Magnetic Spectroscopy Imaging to Evaluate Primary Lateral Sclerosis, Hereditary Spastic Paraplegia and Amyotrophic Lateral Sclerosis
NCT00023075 ·Status: COMPLETED
-
PREVENT ALL ALS Study
NCT06581861 ·Status: RECRUITING
-
Studies in Amyotrophic Lateral Sclerosis (ALS) and Other Neurodegenerative Motor Neuron Disorders
NCT05474235 ·Status: RECRUITING
-
A Pilot Study of Biomarkers for Spinal Muscular Atrophy
NCT00756821 ·Status: COMPLETED
-
Methodology Study of Novel Outcome Measures to Assess Progression of ALS
NCT02611674 ·Status: COMPLETED
-
Natural History of Limb Girdle Muscular Dystrophy Type 2A and Type 2E
NCT03488784 ·Status: COMPLETED
-
The Pre-symptomatic Familial Amyotrophic Lateral Sclerosis (Pre-fALS) Study
NCT00317616 ·Status: RECRUITING
-
Muscular Biomarkers in Amyotrophic Lateral Sclerosis
NCT02670226 ·Status: COMPLETED ·Phase: NA
-
Collection of Blood Samples for DNA in Motor Neuron Disease
NCT00362362 ·Status: COMPLETED
-
Validation of Biomarkers in Amyotrophic Lateral Sclerosis (ALS)
NCT00677768 ·Status: COMPLETED
-
Study of Predictive Factors of Progression of Motor Neurone Disease
NCT02360891 ·Status: COMPLETED
-
ALS Research Collaborative
NCT06885918 ·Status: RECRUITING
-
A Study of the Expression of Nogo and Reticulon Genes in Skeletal Muscle of Patients With Amyotrophic Lateral Sclerosis
NCT00213824 ·Status: TERMINATED
-
Spastic Paraplegia - Centers of Excellence Research Network
NCT06553976 ·Status: RECRUITING
-
Spinal Muscular Atrophy (SMA) Biomarkers Study in the Immediate Postnatal Period of Development
NCT01736553 ·Status: COMPLETED
-
A Longitudinal Study of Amyotrophic Lateral Sclerosis (ALS) Biomarkers
NCT01495390 ·Status: COMPLETED
-
Imaging and BioFluid Biomarkers in Amyotrophic Lateral Sclerosis
NCT02559869 ·Status: COMPLETED
-
Target ALS Biomarker Study; Longitudinal Biofluids, Clinical Measures, and At Home Measures
NCT05137665 ·Status: RECRUITING
-
Skeletal Muscle Biomarkers in People With Fragile Sarcolemmal Muscular Dystrophy
NCT01851447 ·Status: ACTIVE_NOT_RECRUITING
-
A Phase 2 Study of ONO-2808 in Patients With Multiple System Atrophy
NCT05923866 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
Biomarker-driven Phenotypic Dissection of Amyotrophic Lateral Sclerosis
NCT06318598 ·Status: RECRUITING
-
A Natural History Study of Patients With GNE Myopathy and GNE-Related Diseases
NCT01417533 ·Status: COMPLETED
-
Characterization of New Phenotypes of Patients With Spinal Muscular Atrophy Treated With SMN Restoring Therapy
NCT06321965 ·Status: RECRUITING ·Phase: NA
-
A Patient Centric Motor Neuron Disease Activities of Daily Living Scale
NCT02852278 ·Status: COMPLETED