Nemaline Myopathy
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CLINICAL_TRIALS research · 2026-04-13Clinical Trial Update: Natural History Study for Patients With Nemaline Myopathy in the UK
This update describes a natural history study of Nemaline Myopathy in the United Kingdom, led by the University of Oxford. The study is curr…
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CLINICAL_TRIALS research · 2026-03-25Clinical Trial Update: Molecular and Genetic Studies of Congenital Myopathies
Boston Children's Hospital is conducting a study on the molecular and genetic basis of several congenital myopathies, and the trial is curre…
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CLINICAL_TRIALS research · 2026-03-25Clinical Trial Update: Natural History Study for Patients With Nemaline Myopathy in Belgium [NA]
This entry describes a natural history study for patients with nemaline myopathy in Belgium. The study is currently not yet recruiting.
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CLINICAL_TRIALS research · 2026-03-23Clinical Trial Update: Natural History Study for Patients With Nemaline Myopathy in Spain
Clinical trial update for a natural history study of Nemaline Myopathy in Spain; currently recruiting to document disease progression and na…
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CLINICAL_TRIALS research · 2025-02-12Clinical Trial Update: WiTNNess - TNNT1 Myopathy Natural History Study
Clinical trial update indicating a natural history study (WiTNNess) for TNNT1-associated myopathy and infantile-onset nemaline rod myopathy …
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CLINICAL_TRIALS research · 2025-01-24Clinical Trial Update: The Prevalence of RYR1-related Disease
A clinical trial assessing how common RYR1-related disease is, covering several congenital myopathies and malignant hyperthermia; the study …
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CLINICAL_TRIALS research · 2025-01-14Clinical Trial Update: Nemaline Myopathy Clinical Research Network (NM-CTRN)
The Nemaline Myopathy Clinical Research Network (NM-CTRN) is listed as not yet recruiting, indicating ongoing research activity for Nemaline…
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CLINICAL_TRIALS research · 2024-08-19Clinical Trial Update: The Natural History and Muscle Fatigability of Patients With Congenital Myopathies.
This clinical trial update describes a study on the natural history and muscle fatigability in patients with congenital myopathies, currentl…