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KUL0401: An Open-label Pilot Study of Oxatomide in Steroid-Naive Duchenne Muscular Dystrophy - Article


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Muscular dystrophy, Duchenne and Becker types

DBMD; Duchenne/Becker muscular dystrophy


Clinical Trial: KUL0401: An Open-label Pilot Study of Oxatomide in Steroid-Naive Duchenne Muscular Dystrophy

This study is no longer recruiting patients.

Sponsored by: Cooperative International Neuromuscular Research Group
Information provided by: Cooperative International Neuromuscular Research Group

Purpose

This study will help to determine the safety and efficacy of the mast cell stabilizer Oxatomide as a treatment for Duchenne muscular dystrophy (DMD). Boys with DMD who are enrolled in this study will should not have taken steroids to treat DMD for at least twelve months, and should not have taken any nutritional supplements for at least three months. Subjects will complete a two screening visits within a one-week period, and if enrolled will then have their strength tested monthly for three months before beginning therapy with Oxatomide. Once Oxatomide therapy is started, participants will have their strength tested monthly for six months. Following the six month treatment period, participants will be given the option to remain on Oxatomide until the study is completed.

Condition Treatment or Intervention Phase
Muscular Dystrophy, Duchenne
 Drug: Oxatomide (tinset)
Phase II

MedlinePlus related topics:  Muscular Dystrophy
Genetics Home Reference related topics:  muscular dystrophy, Duchenne and Becker types

Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study

Further Study Details: 

Expected Total Enrollment:  15

Study start: January 2002

Eligibility

Ages Eligible for Study:  5 Years   -   10 Years,  Genders Eligible for Study:  Male

Criteria

Subject Inclusion Criteria

1. 5 to 10 years of age

2. ambulatory

3. diagnosis of DMD confirmed by at least one of the following:

  • Positive x-linked family history of DMD in older male relatives (onset by 5 years, wheelchair bound by 12 years), or;
  • Dystrophin immunofluorescence and/or immunoblot showing complete dystrophin deficiency, and clinical picture consistent with typical DMD, or;
  • Gene deletion test positive (missing one or more exons) in the central rod domain (exons 25-60) of dystrophin, where reading frame can be predicted as ‘out of frame’, and clinical picture consistent with typical DMD.

4. glucocorticosteroid-naive (i.e. has not been treated with prednisone or deflazacort within the past year)

5. Evidence of muscle weakness by MRC score or clinical functional evaluation

6. QMT biceps score variability no greater than 10% between screening visits

Subject Exclusion Criteria

1. Failure to achieve one or more of the inclusion criteria listed above

2. Inability to suitably cooperate with strength assessments

3. Symptomatic DMD carrier

4. Use of oxatomide (or other anti-histamine drugs) within the last 6 months for DMD or any other disease

5. Use of creatine monohydrate or glutamine within the last 6 months

6. Use of carnitine, Coenzyme Q10, other amino acids or any herbal medications within the last 3 months

7. History of symptomatic cardiomyopathy

8. History of impairment of hepatic function

9. History of significant concomitant illness or significant impairment of renal function.


Location Information


District of Columbia
      Children's National Medical Center, Washington,  District of Columbia,  20010,  United States

More Information

The Cooperative International Neuromuscular Research Group

Study ID Numbers:  KUL0401
Record last reviewed:  January 2005
Last Updated:  January 26, 2005
Record first received:  April 10, 2002
ClinicalTrials.gov Identifier:  NCT00033813
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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October 10, 2008



Page Updated: September 6, 2005
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