Safety, Tolerability and Effects of L-Arginine in Boys With Dystrophinopathy on Corticosteroids

Mass General Brigham

Status and phase: Completed; Phase 1

Conditions: Becker's Muscular Dystrophy; Dystrophinopathy; Duchenne Muscular Dystrophy

Treatments: Drug: L-arginine

Study type: Interventional

Funder types: Other

Identifiers

NCT01388764

2011D001591

Details and patient eligibility

About

The purpose of the study is to assess the safety, tolerability, and effects of L-Arginine on muscles in boys with dystrophinopathy on corticosteroids. Specifically, to see if L-arginine reduces muscle signal abnormalities on MRI done pre and post 30 days of L-arginine administration.

Full description

Dystrophinopathy is a muscular dystrophy (includes Duchenne or Becker's Muscular Dystrophy) that can be a lethal muscle disorder resulting from defects in the gene for dystrophin, a structural protein required to maintain muscle integrity. Absence of functional dystrophin leaves the muscle membrane vulnerable to damage during contraction. This damage can be exacerbated by an inflammatory response leading to myofiber necrosis.

L-arginine is a widely available dietary supplement amino acid postulated to affect dystrophinopathy in several favorable ways: upregulation of utrophin, vasodilation in muscle via nitric oxide, enhanced synthesis of creatine, increase levels of growth hormone.

We hypothesize that administration of L-arginine may increase levels of creatine and growth hormone and in turn reduce the extent of myofiber damage in our patients with dystrophinopathy

Enrollment: 7 patients

Sex: Male

Ages: 7 to 11 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Confirmation of diagnosis of dystrophinopathy, documented by clinical exam and dystrophin DNA mutation analysis
• Ambulatory male subjects between the ages of 7-11 years
• Stable dosage of corticosteroids for 3 months prior to entry (Screening/Baseline Day 0) and during treatment period
• Able to follow instructions and give assent
• Able to complete nonsedated MR

Exclusion criteria

• Presence of metallic orthopedic hardware in the lower extremity that could affect MRI/MRS measurements
• Routine MRI exclusion criteria such as the presence of a pacemaker, cochlear implant, or cerebral aneurysm clip
• Subjects not capable of cooperating during MR examination
• Known hypersensitivity to L-arginine
• Exposure to another investigational agent, investigational supplements, growth hormone within 3 months prior to entry (Screening/Baseline Day 0) or during treatment period
• Subjects must not be taking L-arginine for at least 4 weeks prior to entry (Day 0)
• Subjects who are non-ambulatory or with daytime ventilatory dependence

Trial design

7 participants in 1 patient group

L-arginine

Experimental group

Treatment:

Drug: L-arginine