Clinical Trials Logo

Hereditary Spastic Paraplegia clinical trials

View clinical trials related to Hereditary Spastic Paraplegia.

Filter by:
  • Enrolling by invitation  
  • Page 1

NCT ID: NCT02327845 Enrolling by invitation - Clinical trials for Amyotrophic Lateral Sclerosis

Phenotype, Genotype & Biomarkers in ALS and Related Disorders

Start date: April 2015
Phase:
Study type: Observational

The goals of this study are: (1) to better understand the relationship between the phenotype and genotype of amyotrophic lateral sclerosis (ALS) and related diseases, including primary lateral sclerosis (PLS), hereditary spastic paraplegia (HSP), progressive muscular atrophy (PMA), and frontotemporal dementia (FTD); and (2) to develop biomarkers that might be useful in aiding therapy development for this group of disorders.