Measuring Levels of SMN in Blood Samples of SMA Patients

Study Identifier:
030203
ClinicalTrials.gov Identifier:
EudraCT Identifier:
N/A
EU CT Number:
N/A
Sponsor:
National Institute of Neurological Disorders and Stroke (NINDS)
Study Complete

Study Details

Medical Condition
  • All Spinal Muscular Atrophies
Study Drug
    Date
    May 2003 - N/A
    Patient Requirements
    Sex: Female & Male
    Age: 2+ years
    Requirements Information

    Protocol Summary

    Spinal muscular atrophy (SMA) is a disorder that affects the motor neurons. SMA is caused by a mutation in a part of the DNA called the survival motor neuron (SMN1) gene, which normally produces a protein called SMN. Because of their gene mutation, people with SMA make less SMN protein, which results in the loss of motor neurons. SMA symptoms may be improved by increasing the levels of SMN protein. The purpose of this study is to determine whether a drug called a histone deacetylase inhibitor can increase SMN levels.

    After undergoing a general medical and neurological evaluation, study participants will donate a blood sample. Researchers will use this sample to measure SMN levels. They will also isolate cells from the blood and treat the cells with various drugs that may increase SMN levels.

    Trial Locations

    Location
    Status
    Location
    National Institutes of Health Clinical Center, 9000 Rockville Pike
    Bethesda, Maryland, United States, 20892
    Status
    N/A

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