CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 12 enrolled
Drug / intervention
alglucosidase alfabiological
Likely dose
alglucosidase alfa 20 mg/kgfrom 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/NCT00486889
NCT00486889Phase 4Completed

A Long-term Study to Evaluate Growth and Development Outcomes in Patients With Infantile-Onset Pompe Disease Who Are Receiving Alglucosidase Alfa

Genzyme, a Sanofi Company·interventional·Posted Jun 15, 2007·Updated Aug 26, 2022

In Brief

A Phase 4 clinical trial evaluating alglucosidase alfa for Pompe Disease and 2 related conditions. Completed, enrolled 12 participants across 3 sites.

Detailed Summary

Pompe disease (also known as glycogen storage disease Type II) is a rare autosomal recessive metabolic muscle disease caused by the deficiency of acid α glucosidase (GAA), an enzyme that degrades lysosomal glycogen. As opposed to the exclusively cytoplasmic accumulation of glycogen that occurs in other glycogen storage disorders, Pompe disease is characterized by organelle bound (lysosomal) and extra-lysosomal accumulation of glycogen in many body tissues, ultimately leading to multisystemic pathology. The overall objective of this study was to evaluate the long-term growth and development of participants with infantile-onset Pompe disease with alglucosidase alfa before 1 year of age. Participants were to be followed for a 10-year period.

Study Details

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

Timeline

Phase 4CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJun 15, 2007
Enrollment StartAug 26, 2008
Primary CompletionNov 23, 2021
TodayJul 2, 2026
Enrollment to primary: 13.2 yearsPosted 19.0 years ago

Interventions

alglucosidase alfabiological

Dose: 20 mg/kg every 2 weeks; Route of administration: Intravenous infusion