A Randomized, Double-Blind, Placebo-Controlled, Global Phase 3 Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy: Results of the PolarisDMD Trial.
J Neuromuscul Dis
; 8(5): 769-784, 2021.
Article
em En
| MEDLINE
| ID: mdl-34120912
ABSTRACT
BACKGROUND:
Edasalonexent (CAT-1004) is an orally-administered novel small molecule drug designed to inhibit NF-κB and potentially reduce inflammation and fibrosis to improve muscle function and thereby slow disease progression and muscle decline in Duchenne muscular dystrophy (DMD).OBJECTIVE:
This international, randomized 2ââ1, placebo-controlled, phase 3 study in patients ≥4â-â<â8 years old with DMD due to any dystrophin mutation examined the effect of edasalonexent (100âmg/kg/day) compared to placebo over 52 weeks.METHODS:
Endpoints were changes in the North Star Ambulatory Assessment (NSAA; primary) and timed function tests (TFTs; secondary). Assessment of health-related function used the Pediatric Outcomes Data Collection tool (PODCI).RESULTS:
One hundred thirty one patients received edasalonexent (nâ=â88) and placebo (nâ=â43). At week 52, differences between edasalonexent and placebo for NSAA total score and TFTs were not statistically significant, although there were consistently less functional declines in the edasalonexent group. A pre-specified analysis by age demonstrated that younger patients (≤6.0 years) showed more robust and statistically significant differences between edasalonexent and placebo for some assessments. Treatment was well-tolerated and the majority of adverse events were mild, and most commonly involved the gastrointestinal system (primarily diarrhea).CONCLUSIONS:
Edasalonexent was generally well-tolerated with a manageable safety profile at the dose of 100âmg/kg/day. Although edasalonexent did not achieve statistical significance for improvement in primary and secondary functional endpoints for assessment of DMD, subgroup analysis suggested that edasalonexent may slow disease progression if initiated before 6 years of age. (NCT03703882).Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Salicilamidas
/
Ácidos Araquidônicos
/
Distrofia Muscular de Duchenne
Tipo de estudo:
Clinical_trials
Limite:
Child
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Child, preschool
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Humans
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Male
Idioma:
En
Revista:
J Neuromuscul Dis
Ano de publicação:
2021
Tipo de documento:
Article
País de afiliação:
Estados Unidos