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Spinal Muscular Atrophy clinical trials

View clinical trials related to Spinal Muscular Atrophy.

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NCT ID: NCT00481013 Completed - Clinical trials for Spinal Muscular Atrophy

Valproic Acid in Ambulant Adults With Spinal Muscular Atrophy

VALIANTSMA
Start date: July 2007
Phase: Phase 2
Study type: Interventional

The primary objective of this proposal is to determine whether oral VPA is effective in treating SMA in adult patients.

NCT ID: NCT00443066 Completed - Clinical trials for Spinal Muscular Atrophy

Clinical Study of Spinal Muscular Atrophy

Start date: May 2005
Phase:
Study type: Observational

The investigators propose to prepare for clinical trials where SMA patients are asked to join the research effort. The visits will include questions, physical exam, blood drawing, and sometimes X-rays and a skin biopsy. The investigators will use modern computer methods to process the information during which the investigators will plan a clinical trial. Once the clinical trial begins, the investigators will offer SMA patients participation if they meet the criteria for that trial. Identifying an effective SMA treatment is very important because there is currently none. Clinical trials are the only way to decide whether a new treatment works in SMA patients or not.

NCT ID: NCT00374075 Completed - Clinical trials for Spinal Muscular Atrophy

Study of Safety and Dosing Effect on SMN Levels of Valproic Acid (VPA) in Patients With Spinal Muscular Atrophy

Start date: September 2003
Phase: Phase 1
Study type: Interventional

This is an open label phase I/II clinical trial to assess safety, tolerability and potential effect on SMN mRNA and protein in vivo of a compound in which preliminary evidence supports a potential effect on SMN levels in vitro.

NCT ID: NCT00227266 Completed - Clinical trials for Spinal Muscular Atrophy

Valproic Acid and Carnitine in Patients With Spinal Muscular Atrophy

Start date: September 2005
Phase: Phase 2
Study type: Interventional

This is a multi-center trial to assess safety and efficacy of a combined regimen of oral valproic acid (VPA) and carnitine in patients with Spinal Muscular Atrophy (SMA) 2 to 17 years of age. Cohort 1 is a double-blind placebo-controlled randomized intention to treat protocol for SMA "sitters" 2 - 8 years of age. Cohort 2 is an open label protocol for SMA "standers and walkers" 3 - 17 years of age to explore responsiveness of efficacy outcomes. Outcome measures will include blood chemistries, functional testing, pulmonary function testing, electrophysiological evaluations, PedsQL quality of life assessment, quantitative assessments of survival motor neuron (SMN) mRNA from blood samples, growth and vital sign parameters. Six centers will enroll a total of 90 patients.

NCT ID: NCT00061607 Completed - Clinical trials for Spinal Muscular Atrophy

Measuring Levels of SMN in Blood Samples of SMA Patients

Start date: May 19, 2003
Phase: N/A
Study type: Observational

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.

NCT ID: NCT00004771 Completed - Clinical trials for Amyotrophic Lateral Sclerosis

Phase II Study of Leuprolide and Testosterone for Men With Kennedy's Disease or Other Motor Neuron Disease

Start date: October 1992
Phase: Phase 2
Study type: Interventional

OBJECTIVES: I. Evaluate the effects of androgen suppression with leuprolide and androgen replacement with testosterone enanthate on muscle strength in men with Kennedy's disease or other motor neuron disease.