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

Primary Purpose

Muscular Dystrophy, Duchenne

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Oxatomide (tinset)
Sponsored by
Cooperative International Neuromuscular Research Group
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Muscular Dystrophy, Duchenne focused on measuring Duchenne, muscular, dystrophy, controlled clinical trial, CINRG

Eligibility Criteria

5 Years - 10 Years (Child)MaleDoes not accept healthy volunteers

Subject Inclusion Criteria 5 to 10 years of age ambulatory 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. glucocorticosteroid-naive (i.e. has not been treated with prednisone or deflazacort within the past year) Evidence of muscle weakness by MRC score or clinical functional evaluation QMT biceps score variability no greater than 10% between screening visits Subject Exclusion Criteria Failure to achieve one or more of the inclusion criteria listed above Inability to suitably cooperate with strength assessments Symptomatic DMD carrier Use of oxatomide (or other anti-histamine drugs) within the last 6 months for DMD or any other disease Use of creatine monohydrate or glutamine within the last 6 months Use of carnitine, Coenzyme Q10, other amino acids or any herbal medications within the last 3 months History of symptomatic cardiomyopathy History of impairment of hepatic function History of significant concomitant illness or significant impairment of renal function.

Sites / Locations

  • Children's National Medical Center

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
April 10, 2002
Last Updated
March 7, 2014
Sponsor
Cooperative International Neuromuscular Research Group
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1. Study Identification

Unique Protocol Identification Number
NCT00033813
Brief Title
KUL0401: An Open-label Pilot Study of Oxatomide in Steroid-Naive Duchenne Muscular Dystrophy
Study Type
Interventional

2. Study Status

Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
January 2002 (undefined)
Primary Completion Date
December 2006 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Cooperative International Neuromuscular Research Group

4. Oversight

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Muscular Dystrophy, Duchenne
Keywords
Duchenne, muscular, dystrophy, controlled clinical trial, CINRG

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
15 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Oxatomide (tinset)

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
10 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Subject Inclusion Criteria 5 to 10 years of age ambulatory 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. glucocorticosteroid-naive (i.e. has not been treated with prednisone or deflazacort within the past year) Evidence of muscle weakness by MRC score or clinical functional evaluation QMT biceps score variability no greater than 10% between screening visits Subject Exclusion Criteria Failure to achieve one or more of the inclusion criteria listed above Inability to suitably cooperate with strength assessments Symptomatic DMD carrier Use of oxatomide (or other anti-histamine drugs) within the last 6 months for DMD or any other disease Use of creatine monohydrate or glutamine within the last 6 months Use of carnitine, Coenzyme Q10, other amino acids or any herbal medications within the last 3 months History of symptomatic cardiomyopathy History of impairment of hepatic function History of significant concomitant illness or significant impairment of renal function.
Facility Information:
Facility Name
Children's National Medical Center
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20010
Country
United States

12. IPD Sharing Statement

Links:
URL
http://www.cnmcresearch.org/cinrg/index.asp
Description
The Cooperative International Neuromuscular Research Group

Learn more about this trial

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

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