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Clinical trial

The Natural History of Patients With Congenital Muscular Dystrophies Due to Mutations in the SELENON or LAMA2 Genes: Working Towards Trial-readiness in Two Mitochondrial Myopathy Mimics

NCT04478981 is registered in ClinicalTrials.gov with Radboud University Medical Center as lead sponsor.

NCT NCT04478981
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Registry record

As filed in ClinicalTrials.gov.

Title
The Natural History of Patients With Congenital Muscular Dystrophies Due to Mutations in the SELENON or LAMA2 Genes: Working Towards Trial-readiness in Two Mitochondrial Myopathy Mimics
Lead sponsor
Radboud University Medical Center
Phase
Observational
Overall status
Completed
Start date
August 26, 2020
Completion date
March 24, 2023
Enrollment
38 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

mdc1a, selenon-related myopathy