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

NCT ID: NCT00033813

Last Updated: 2014-03-10

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 15 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2002-01-31

Brief Summary

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.

Conditions

Muscular Dystrophy, Duchenne

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Interventions

Oxatomide (tinset)

Intervention Type: DRUG

Eligibility Criteria

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

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.

• Minimum Eligible Age: 5 Years
• Maximum Eligible Age: 10 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

Cooperative International Neuromuscular Research Group

NETWORK

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Children's National Medical Center

Washington D.C., District of Columbia, United States

Countries

United States

Related Links

http://www.cnmcresearch.org/cinrg/index.asp

The Cooperative International Neuromuscular Research Group

Other Identifiers

KUL0401

Identifier Type: -

Identifier Source: org_study_id