Safety and clinical activity of elosulfase alfa in pediatric patients with Morquio A syndrome (mucopolysaccharidosis IVA) less than 5 y

Pediatr Res. 2015 Dec;78(6):717-22. doi: 10.1038/pr.2015.169. Epub 2015 Sep 2.

Abstract

Background: Previous studies have shown that elosulfase alfa has a favorable efficacy/safety profile in Morquio A patients aged ≥5 y. This study evaluated safety and impact on urine keratan sulfate (uKS) levels and growth velocity in younger patients.

Methods: Fifteen Morquio A patients aged <5 y received elosulfase alfa 2.0 mg/kg/week for 52 wk during the primary treatment phase of a phase II, open-label, multinational study. Primary endpoint was safety and tolerability; secondary endpoints were change in uKS and growth velocity over 52 wk.

Results: All 15 patients completed the primary treatment phase. Six of 743 infusions (0.8%) administered led to adverse events (AEs) requiring infusion interruption and medical intervention. Eleven patients (73.3%) had ≥1 study drug-related AE, mostly infusion-associated reactions. Mean z-score growth rate per year numerically improved from -0.6 at baseline to -0.4 at week 52. Comparison to untreated subjects of similar age in the Morquio A Clinical Assessment Program study showed a smaller decrease in height z-scores for treated than for untreated patients. Mean percent change from baseline in uKS was -30.2% at 2 wk and -43.5% at 52 wk.

Conclusion: Early intervention with elosulfase alfa is well-tolerated and produces a decrease in uKS and a trend toward improvement in growth.

Trial registration: ClinicalTrials.gov NCT01515956.

Publication types

  • Clinical Trial, Phase II
  • Multicenter Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Biomarkers / urine
  • Body Height / drug effects
  • Child Development / drug effects
  • Child, Preschool
  • Chondroitinsulfatases / administration & dosage*
  • Chondroitinsulfatases / adverse effects
  • Drug Administration Schedule
  • Early Medical Intervention
  • Enzyme Replacement Therapy* / adverse effects
  • Europe
  • Female
  • Humans
  • Infant
  • Infusions, Intravenous
  • Keratan Sulfate / urine
  • Male
  • Mucopolysaccharidosis IV / diagnosis
  • Mucopolysaccharidosis IV / drug therapy*
  • Mucopolysaccharidosis IV / enzymology
  • Mucopolysaccharidosis IV / physiopathology
  • Mucopolysaccharidosis IV / urine
  • Recombinant Proteins / administration & dosage
  • Time Factors
  • Treatment Outcome
  • United Kingdom

Substances

  • Biomarkers
  • Recombinant Proteins
  • Keratan Sulfate
  • Chondroitinsulfatases
  • GALNS protein, human

Associated data

  • ClinicalTrials.gov/NCT01515956