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Natural History of Pompe Disease
Sponsor: Assistance Publique - Hôpitaux de Paris
Summary
The project is a prospective study in which patients affected by adult-onset Pompe disease with c.-32-13T\>G mutation in the GAA gene will be followed-up during two years to describe the natural history using clinical, imaging, histological and molecular parameters. Secondary objectives are: * To identify biomarkers for assessing efficacy of future therapies based on correcting aberrant alternative splicing in Pompe patients with c.-32-13T\>G mutations. * To determine effectiveness of antisense oligonucleotide chemistries to restore full length GAA transcripts, GAA protein and GAA enzyme activity in fibroblasts and myoblasts obtained from skin and muscle biopsies as well as leucocytes of Pompe patients with c.-32-13T\>G mutations.
Official title: Clinical and Molecular Aspects of Adult Onset Pompe Disease: a Natural History Study
Key Details
Gender
All
Age Range
18 Years - 80 Years
Study Type
OBSERVATIONAL
Enrollment
20
Start Date
2019-06-07
Completion Date
2033-03
Last Updated
2024-04-08
Healthy Volunteers
No
Conditions
Locations (1)
Hôpital Raymond Poincaré
Garches, Hauts-de-Seine, France