CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 31 enrolled
Drug / intervention
Edasalonexent +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02439216
NCT02439216Phase 2Completed

A Phase 1/2 Study of Edasalonexent (CAT-1004) in Pediatric Patients With Duchenne Muscular Dystrophy

Catabasis Pharmaceuticals·interventional·Posted May 8, 2015·Updated Sep 23, 2022

In Brief

A Phase 2 clinical trial evaluating Edasalonexent and Placebo for Muscular Dystrophy, Duchenne. Completed, enrolled 31 participants across 5 sites.

Detailed Summary

The MoveDMD study is a 3-part, Phase 1/2, multi-site study to evaluate the safety, efficacy, pharmacokinetics (PK) and pharmacodynamics (PD) of edasalonexent (also known as CAT-1004) in pediatric patients with a genetically confirmed diagnosis of DMD. Male patients from ≥4 to \<8 years of age will be enrolled. Edasalonexent is an orally administered small molecule targeted to inhibit activated NF-κB, a molecule that is activated from infancy in DMD and which is central to causing muscle damage and preventing muscle regeneration. Data on magnetic resonance imaging of the lower and upper leg muscles, physical function (including timed function tests) and muscle strength will be studied.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20162017201820192020202120222023202420252026
First PostedMay 8, 2015
Enrollment StartApr 1, 2016
Primary CompletionJan 12, 2017
Study CompletionAug 1, 2019
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 11.2 years ago

Interventions

Edasalonexentdrug

Placebodrug