Safety and Efficacy Evaluation of Repeat neoGAA Dosing in Late Onset Pompe Disease Patients.
Pompe Disease, Glycogen Storage Disease Type II (GSD II), Acid Maltase Deficiency
About this trial
This is an interventional treatment trial for Pompe Disease
Eligibility Criteria
Inclusion criteria :
For both Group 1 and Group 2:
- Male or female patients with confirmed acid α-glucosidase (GAA) enzyme deficiency from any tissue source and/or confirmed GAA gene mutation and without known cardiac hypertrophy.
- Patient willing and able to provide signed informed consent
- Patient is able to ambulate 50 meters (approximately 160 feet) without stopping and without an assistive device. Use of assistive device for community ambulation is appropriate.
- Patient has a forced vital capacity (FVC) in upright position of ≥50% predicted.
- The patient, if female and of childbearing potential, must have a negative pregnancy test [urine beta-human chorionic gonadotropin (β-hCG)] at baseline.
Group 2 patients only:
- The patient has been previously treated with alglucosidase alfa for at least 9 months.
Exclusion criteria:
For both Group 1 and Group 2:
- Patient is wheelchair dependent.
- Patient requires invasive-ventilation (non-invasive ventilation is allowed).
- Patient is participating in another clinical study using investigational treatment.
- Patient, in the opinion of the Investigator, is unable to adhere to the requirements of the study.
- Patient has clinically significant organic disease (with the exception of symptoms relating to Pompe disease), including clinically significant cardiovascular, hepatic, pulmonary, neurologic, or renal disease, or other medical condition, serious intercurrent illness, or extenuating circumstance that, in the opinion of the Investigator, precludes participation in the study or potentially decreases survival.
- Patient cannot submit to MRI examination because of a formal contraindication such as a pacemaker, implanted ferromagnetic metals, anxiety disorder, etc.
Group 1 only:
- Patient has had previous treatment with alglucosidase alfa or any other enzyme replacement therapy (ERT) for Pompe disease.
Group 2 only:
- Patient has a high risk for a severe allergic reaction to neoGAA (i.e. previous moderate to severe anaphylactic reaction to alglucosidase alfa and/or patient has immunoglobulin (Ig) E antibodies to alglucosidase alfa, and/or a history of sustained high immunoglobulin G (IgG) antibody titers to alglucosidase alfa that in the opinion of the investigator suggest a high risk for an allergic reaction to neoGAA).
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Sites / Locations
- Investigational Site Number 840006
- Investigational Site Number 840010
- Investigational Site Number 840001
- Investigational Site Number 840008
- Investigational Site Number 840002
- Investigational Site Number 840009
- Investigational Site Number 840003
- Investigational Site Number 056001
- Investigational Site Number 208001
- Investigational Site Number 250001
- Investigational Site Number 250003
- Investigational Site Number 250002
- Investigational Site Number 276003
- Investigational Site Number 276001
- Investigational Site Number 276002
- Investigational Site Number 528001
- Investigational Site Number 826003
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm 6
Experimental
Experimental
Experimental
Experimental
Experimental
Experimental
GZ402666 (neoGAA) Group 1 - 5 mg
GZ402666 (neoGAA) Group 1 - 10 mg
GZ402666 (neoGAA) Group 1 - 20 mg
GZ402666 (neoGAA) Group 2 - 5 mg
GZ402666 (neoGAA) Group 2 - 10 mg
GZ402666 (neoGAA) Group 2 - 20 mg
Intravenous infusion of 5mg neoGAA to treatment naïve late onset Pompe disease patients once every other week for a total of 24 weeks
Intravenous infusion of 10mg neoGAA to treatment naïve late onset Pompe disease patients once every other week for a total of 24 weeks.
Intravenous infusion of 20mg neoGAA to treatment naïve late onset Pompe disease patients once every other week for a total of 24 weeks.
Intravenous infusion of 5mg neoGAA once every other week for a total of 24 weeks to late onset Pompe disease patients previously treated with alglucoside alfa.
Intravenous infusion of 10mg neoGAA once every other week for a total of 24 weeks to late onset Pompe disease patients previously treated with alglucoside alfa.
Intravenous infusion of 20mg neoGAA once every other week for a total of 24 weeks to late onset Pompe disease patients previously treated with alglucoside alfa.