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Clinical trial

WiTNNess: An International Natural History Study of Autosomal Recessive TNNT1 Myopathy

NCT06374719 is registered in ClinicalTrials.gov with Clinic for Special Children as lead sponsor.

NCT NCT06374719
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Registry record

As filed in ClinicalTrials.gov.

Title
WiTNNess: An International Natural History Study of Autosomal Recessive TNNT1 Myopathy
Lead sponsor
Clinic for Special Children
Phase
Observational
Overall status
Recruiting
Start date
September 23, 2018
Completion date
June 1, 2027
Enrollment
40 (estimated)
Sites
1

Conditions

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

amish nemaline myopathy, anm, genetic muscle disease, infantile-onset nemaline rod myopathy, myopathies, nemaline, myopathy, myopathy, rod, myopathy; hereditary, nem5, nemaline myopathy 5, recessive hereditary disorder (autosomal), tnnt1-associated myopathy