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 overall objective is to evaluate the safety and efficacy of rhGAA in patients with advanced Late-onset Pompe disease.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
5
20 mg/kg qow
Hopital Raymond Poincare
Garches, France
Treatment effect on muscle strength and functional status.
Time frame: six months and one year
Treatment effect on pulmonary function and/or ventilation conditions.
Time frame: six months and one year
Treatment effect on cardiomyopathy noted at inclusion
Time frame: six months and one year
Treatment effect on fatigue.
Time frame: six months and one year
Treatment effect on quality of life.
Time frame: six months and one year
Treatment effect on muscular atrophy.
Time frame: six months and one year
Overall patient satisfaction with treatment (visual analog scale).
Time frame: six months and one year
Pharmacodynamics assessment.
Time frame: six months and one year
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