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Nemaline Myopathy
Clinical trial pipeline · Data from ClinicalTrials.gov
See which Nemaline Myopathy trials may be worth asking aboutClinical trial pipeline · Data from ClinicalTrials.gov
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WiTNNess is designed to accurately document the natural course and variation of muscle disease caused by pathogenic changes of the TNNT1 gene. The primary aim o…
In the Congenital Myopathy Research Program at Boston Children's Hospital and Harvard Medical School, the researchers are studying the congenital myopathies (ne…
The objective of this natural history study is to comprehensively characterize the disease progression and clinical features of nemaline myopathies. The study a…
This single-arm pilot study evaluates the effects of whole-body electrical muscle stimulation (WB-EMS) exercise on neuromuscular and physical function in adults…
Core myopathies (CCD/MmD), nemaline myopathies (NEM) and centronuclear myopathies (CNM) are three types of rare congenital myopathies. Not much is known about t…
The goal of this study is to to learn more about what assessments would be useful to measure for NM and what normally happens during the lives of people with NM…
This is a prospective, longitudinal, observational study designed to characterize the natural history of Nemaline Myopathy (NM), a rare congenital neuromuscular…