Mechanisms of Cell Death in Spinal Muscular Atrophy

Study Identifier:
82008
ClinicalTrials.gov Identifier:
EudraCT Identifier:
N/A
EU CT Number:
N/A
Sponsor:
Nemours Children's Clinic
Study Complete

Study Details

Medical Condition
  • All Spinal Muscular Atrophies
Study Drug
    Date
    May 2008 - Feb 2020
    Patient Requirements
    Sex: Female & Male
    Age: N/A - 21 Years
    Requirements Information

    Protocol Summary

    Spinal muscular atrophy is a genetically based disease that affects motor neurons in the spinal cord and leads to muscle wasting and weakness. The gene found to be responsible for the underlying disease is called the SMN or survival motor neuron gene. Individuals with SMA are either missing a copy of the gene or have a mutation in the gene. Although the gene has been identified, how it actually causes the motor neurons to die and leads to muscle wasting and weakness is not completely understood. The investigators have found that skin cells from children with SMA tend to be more susceptible to cell death when exposed to cell death inducing agents. In this protocol, The investigators wish to study the mechanisms by which these cells die when exposed to these agents and how this may be related to the gene defect and the disease.

    Trial Locations

    Location
    Status
    Location
    Alfred I. duPont Hospital for Children
    Wilmington, Delaware, United States, 19803
    Status
    N/A
    Location
    Nemours Children's Specialty Care, Jacksonville
    Jacksonville, Florida, United States, 32207
    Status
    N/A

    Contact Cure SMA

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