Summary

Eligibility
for males ages 6-14 (full criteria)
Location
at UC Davis UCLA
Dates
study started
completion around

Description

Summary

The FOX study is a 2-part, multicenter, Phase 2 study of safety, pharmacokinetics, and biomarkers in children and adolescents with Duchenne muscular dystrophy previously treated with gene therapy including a randomized, double-blind, placebo-controlled Part A, followed by an open-label part B.

Official Title

A Phase 2 Study to Evaluate the Effect of EDG-5506 on Safety, Pharmacokinetics, and Biomarkers in Children and Adolescents With Duchenne Muscular Dystrophy Previously Treated With Gene Therapy

Details

FOX is a 2-part, multi-center, Phase 2 study to evaluate the effect of EDG-5506 on safety, pharmacokinetics and biomarkers of muscle damage in approximately 24 children and adolescents with Duchenne muscular dystrophy treated with oral, once-daily EDG-5506.This study will have up to a 4-week Screening period, a 12-week randomized double-blind, placebo-controlled treatment period (Part A), followed by a 40-week open-label extension period (Part B) .

Approximately twenty-four (24) participants aged 6 to 14, inclusive, will be randomized to EDG-5506 or placebo in a 2:1 ratio. Two dose cohorts (Cohort 1 and Cohort 2) of approximately 12 participants each will be enrolled.

Keywords

Duchenne Muscular Dystrophy, Muscular Dystrophies, EDG-5506 Dose 1, EDG-5506 Dose 2

Eligibility

You can join if…

Open to males ages 6-14

  • Aged 6 to 14 with a documented mutation on the DMD gene and phenotype consistent with DMD.
  • Prior receipt of an AAV-based gene therapy (≥ 2 years after study drug administration in an open-label study or ≥ 3 years after randomization in a randomized study).
  • Able to complete stand from supine in ≤ 8 seconds at the Screening visit and able to perform the 4-stair climb in < 10 seconds at the Screening visit.
  • Body weight ≥ 20 kg at the Screening visit.
  • Treatment with a stable dose of corticosteroids for a minimum of 6 months prior to the Baseline visit.

You CAN'T join if...

  • Medical history or clinically significant physical exam/laboratory result that, in the opinion of the investigator, would render the participant unsuitable for the study. This includes venous access that would be too difficult to facilitate repeated blood sampling.
  • Screening visit cardiac echocardiography showing left ventricular ejection fraction (LVEF) < 40%.
  • Receipt of an investigational drug (other than the AAV-based gene therapy per Inclusion criteria) within 30 days or 5 half-lives (whichever is longer) of the Screening visit in the present study.
  • Receipt of an exon-skipping therapy within 6 months prior to the Screening visit.

Locations

  • UCLA Medical Center accepting new patients
    Los Angeles California 90095 United States
  • UC Davis Medical Center accepting new patients
    Sacramento California 95817 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Edgewise Therapeutics, Inc.
Links
Sponsor Website
ID
NCT06100887
Phase
Phase 2 Duchenne Muscular Dystrophy Research Study
Study Type
Interventional
Participants
Expecting 24 study participants
Last Updated