multiple acyl-CoA dehydrogenase deficiency
multiple acyl-CoA dehydrogenase deficiency
Explore linked clinical trials. Standard reference: MONDO:00092822 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Natural History of MADD | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, inborn disorder of amino acid metabolism, inborn errors of metabolism, inborn mitochondrial metabolism disorder, metabolic disease, multiple acyl-CoA dehydrogenase deficiency | Recruiting | Not stated | 2026-09-16 | NCT07734090 | |
| Ganciclovir Resistant/Refractory Cytomegalovirus Infection in SOT Recipients and HSCT Patients | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA Virus Infections, Herpesviridae infectious disease, Infections, Nutritional and Metabolic Diseases, cytomegalovirus infection, hereditary disease, inborn disorder of amino acid metabolism, inborn errors of metabolism, inborn mitochondrial metabolism disorder, metabolic disease, multiple acyl-CoA dehydrogenase deficiency, viral infectious disease | Recruiting | Not stated | 2026-06-15 | NCT05234723 |