Study to Test the Effectiveness and Safety of Experimental Viltolarsen in Ambulant Boys With Duchenne Muscular Dystrophy (DMD)

a study on Duchenne Muscular Dystrophy

Summary

Eligibility
for males ages 4-7 (full criteria)
Location
at Sacramento, California and other locations
Dates
study started
completion

Description

Summary

The main objective of this study is to evaluate the efficacy of Viltolarsen compared to placebo in Duchenne muscular dystrophy (DMD) patients amenable to exon 53 skipping.

Official Title

A Phase 3 Randomized, Double-blind, Placebo-controlled, Multi-center Study to Assess the Efficacy and Safety of Viltolarsen in Ambulant Boys With Duchenne Muscular Dystrophy (DMD)

Details

This is a Phase 3 randomized, double-blind, placebo-controlled, multi-center study to assess the efficacy and safety of Viltolarsen in ambulant boys with Duchenne muscular dystrophy. Eligible patients with out-of-frame deletion mutations amenable to exon 53 skipping will be randomized to receive once weekly intravenous (IV) infusions of 80 mg/kg Viltolarsen or placebo for up to 48 weeks.

The study will enroll approximately 74 patients amenable to exon 53 skipping. Clinical efficacy will be assessed at regularly scheduled study visits, including functional tests such as Time to Stand Test (TTSTAND), Time to Run/Walk 10 Meters Test (TTRW), Six-minute Walk Test (6MWT), North Star Ambulatory Assessment (NSAA), Time to Climb 4 Steps Test (TTCLIMB) and Hand-held dynamometer (elbow extension, elbow flexion, knee extension and knee flexion on the dominant side only).

Safety will be assessed through the collection of adverse events (AEs), laboratory tests, electrocardiograms (ECGs), vital signs, and physical examinations throughout the study.

Blood samples will be taken periodically throughout the study to assess the pharmacokinetics of study drug.

Keywords

Duchenne Muscular Dystrophy, Muscular Dystrophies, Viltolarsen

Eligibility

You can join if…

Open to males ages 4-7

  • Male ≥ 4 years and < 8 years of age
  • Confirmed DMD mutation(s) in the dystrophin gene that is amenable to skipping of exon 53 to restore the dystrophin mRNA reading frame
  • Able to walk independently without assistive devices
  • TTSTAND < 10 seconds
  • Stable dose of glucocorticoid (GC) for at least 3 months prior to study entry and is expected to remain on stable dose of GC treatment for the duration of the study
  • Other inclusion criteria may apply

You CAN'T join if...

  • Current or history of chronic systemic fungal or viral infections
  • Acute illness within 4 weeks prior to the first dose of study drug
  • Evidence of symptomatic cardiomyopathy (Note: Asymptomatic cardiac abnormality on investigation would not be exclusionary)
  • Allergy or hypersensitivity to the study drug or to any of its constituents
  • Severe behavioral or cognitive problems that preclude participation in the study, in the opinion of the investigator
  • Previous or ongoing medical condition, medical history, physical findings or laboratory abnormalities that could affect safety, make it unlikely that treatment and follow-up will be correctly completed or impair the assessment of study results, in the opinion of the investigator;
  • Surgery within the 3 months prior to the first dose of study drug or surgery is planned for anytime during the duration of the study
  • Participant has positive test results for hepatitis B antigen, hepatitis C antibody or human immunodeficiency virus (HIV)
  • Currently taking any other investigational drug or has taken any other investigational drug within 3 months prior to the first dose of study drug or within 5 times the half-life of a medication, whichever is longer
  • Previously enrolled in an interventional study of viltolarsen
  • Currently taking any other exon skipping agent or has taken any other exon skipping agent within 3 months prior to the first dose of study drug
  • Having taken any gene therapy
  • Other exclusion criteria may apply

Locations

  • University of California Davis Medical Center
    Sacramento California 95817 United States
  • Alberta Children's Hospital
    Calgary Canada

Details

Status
accepting new patients
Start Date
Completion Date
Sponsor
NS Pharma, Inc.
Links
Sign up for this study
ID
NCT04060199
Phase
Phase 3 Duchenne Muscular Dystrophy Research Study
Study Type
Interventional
Participants
About 77 people participating
Last Updated
Contact us about this trial