Mode
Text Size
Log in / Sign up
Phase 4 N=13 Randomized Treatment

High Dose or High Dose Frequency Study of Alglucosidase Alfa

Pompe Disease · Glycogen Storage Disease Type II (GSD-II) · Glycogenesis 2 Acid Maltase Deficiency

Enrolled (actual)
13
Serious AEs
25.0%
Results posted
Apr 2011
Primary outcome: Primary: Participants' Efficacy Response During the Treatment Period as Compared to Baseline for Participants With Respiratory Decline on Standard Treatment — 0; 0; 0; 1 participants

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
alglucosidase alfa (Biological)
Age
Pediatric, Adult, Older Adult · 0+ yrs
Sex
All
Sponsor
Genzyme, a Sanofi Company
Primary completion
Dec 2009

Outcome Measures

OutcomeResultp-value
PRIMARY
Participants' Efficacy Response During the Treatment Period as Compared to Baseline for Participants With Respiratory Decline on Standard Treatment
0; 0; 0; 1; 0; 0
PRIMARY
Participants' Efficacy Response During the Treatment Period as Compared to Baseline for Participants With Motor Function Decline on Standard Treatment
2; 4; 1; 2; 1; 0
PRIMARY
Summary of Participants Reporting Treatment-Emergent Adverse Events During the Treatment Period
6; 7; 0; 2; 6; 7
SECONDARY
Baseline Values for Left Ventricular Mass (LVM) Z-Scores
0.3; -0.3
SECONDARY
Change From Baseline in Left Ventricular Mass (LVM) Z-Score at Week 52
0.3; 0.4
SECONDARY
Baseline Values for Left Ventricular Mass Index (LVMI)
62.1; 56.5
SECONDARY
Change From Baseline in Left Ventricular Mass Index (LVMI) at Week 52
12.5; 4.0
SECONDARY
Change From Baseline in Ventilator Use at Last Assessment (Approximately Week 52)
0; 0; 2; 3; 1; 0
SECONDARY
Change From Baseline in Body Strength Measured by the Manual Muscle Testing (MMT) Total Score at Week 52
SECONDARY
Baseline Values of Raw Scores for Gross Motor Function Measure 66 (GMFM-66) Results
65.0; 82.8
SECONDARY
Change From Baseline in Raw Scores for Gross Motor Function Measure 66 (GMFM-66) Results at Week 52
6.0; 6.7
SECONDARY
Baseline Values in Mobility as Measured by the Pompe Pediatric Evaluation of Disability Inventory (Pompe PEDI)
38.3; 46.8
SECONDARY
Change From Baseline in Mobility as Measured by the Pompe Pediatric Evaluation of Disability Inventory (Pompe PEDI) at Week 52
0.6; 3.5
SECONDARY
Baseline Values for Normative Physical Component Summary of Medical Outcomes Study Short Form Health Survey (SF-36)
31.3; 36.0
SECONDARY
Change From Baseline in Normative Physical Component Summary of Medical Outcomes Study Short Form Health Survey (SF-36) at Week 52
2.5; 4.4

Summary

Pompe disease (also known as glycogen storage disease Type II) is caused by a deficiency of a critical enzyme in the body called acid alpha-glucosidase (GAA). Normally, GAA is used by the body's cells to break down glycogen (a stored form of sugar) within specialized structures called lysosomes. In patients with Pompe disease, an excessive amount of glycogen accumulates and is stored in various tissues, especially heart and skeletal muscle, which prevents their normal function. The objective of this exploratory study is to evaluate the safety and efficacy of alternative dosing regimens of alglucosidase alfa in patients with Pompe disease who have not demonstrated an optimal response to the standard dosing regimen of 20 mg/kg every other week after a minimum of 6 months treatment immediately prior to study entry.

Eligibility Criteria

Inclusion Criteria

  • The patient or patient's legal guardian must provide signed, informed consent prior to performing any study-related procedures;
  • The patient must have a clinical diagnosis of Pompe disease as defined by documented GAA deficiency in skin fibroblasts or blood;
  • The patient must have been compliant with the standard dosing regimen of alglucosidase alfa (20 mg/kg every other week) for a minimum of 6 months immediately prior to study entry
  • The patient must have clinical decline or sub-optimal improvement in at least one of the following parameters as compared to their condition prior to the beginning alglucosidase alfa treatment:
  • Cardiac: Left Ventricular Mass (LVM) Z-score ≥6 or LVM index ≥150 g/m2 after a minimum of 6 months of regular treatment with alglucosidase alfa; OR
  • Respiratory: New development of respiratory failure requiring the use of ventilatory assistance (invasive or non-invasive) after a minimum of 6 months of regular treatment with alglucosidase alfa. Ventilatory assistance must have been required for at least 4 weeks prior to study enrollment; OR
  • Motor Skills:
  • For patients ≤ 2 years of age at study entry, failure to acquire at least 2 new gross motor milestones after a minimum of 6 months of regular treatment with alglucosidase alfa; OR
  • For patients > 2 years of age at study entry, worsening of proximal upper extremity muscle weakness as determined by the Investigator through loss of functional use of the upper extremities after a minimum of 6 months of regular treatment with alglucosidase alfa, OR
  • For patients > 8 years of age at study entry, worsening of proximal upper extremity muscle weakness as determined by the Investigator through longitudinal assessments of manual muscle testing after a minimum of 6 months of regular treatment with alglucosidase alfa, OR
  • For patients previously ambulatory, progression to use of an assistive device for ambulation due to worsening of proximal lower extremity muscle weakness after a minimum of 6 months of regular treatment with alglucosidase alfa.

Exclusion Criteria

  • For patients < 18 years of age, negative Cross-Reactive Immunologic Material (CRIM) assay result (added in protocol amendment #2);
  • Any medical condition which, in the opinion of the Investigator, could interfere with treatment or evaluation of safety and/or efficacy of alglucosidase alfa;
  • The patient is not currently receiving alglucosidase alfa;
  • The patient has major congenital abnormality;
  • The patient has used any investigational product (other than alglucosidase alfa in those regions where the product is not commercially available) within 30 days prior to study enrollment;
  • The patient is pregnant or lactating.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00483379). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search