M 3243a G Mutation Causing Mitochondrial Myopathy clinical trials

Explore recruiting m 3243a g mutation causing mitochondrial myopathy clinical trials.

Also recruiting in Europe

M 3243a G Mutation Causing Mitochondrial Myopathy trials registered in the EU Clinical Trials Information System (CTIS). These are outside the "near me" matcher above - open a study for full details.

Assess efficacy of intra-arterial autologous myogenic stam cell therapy for m.3243A>G mutation carriers

Netherlands

Phase I and Phase II (Integrated)- First administration to humans EU CTIS Study details

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Obesity Type 2 diabetes Type 1 diabetes Prediabetes Weight loss Metabolic syndrome High cholesterol High triglycerides High blood pressure PCOS Hypothyroidism Thyroid disease Gout Fatty liver disease (NAFLD/NASH) Heart failure Coronary artery disease Atrial fibrillation Stroke Stroke recovery Peripheral artery disease Pulmonary hypertension Deep vein thrombosis Chronic kidney disease Diabetic kidney disease