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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Clinical and Laboratory Study of Methylmalonic AcidemiaCongenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, hyperhomocysteinemia, inborn disorder of amino acid metabolism, inborn errors of metabolism, inborn organic aciduria, malabsorption syndrome, metabolic disease, methylmalonic acidemia, nutritional deficiency disease, nutritional disorder, vitamin B deficiency, vitamin deficiency disorderRecruitingNot stated2026-10-08NCT00078078

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Research sitesCityCountryLinked trials
Children's National Medical CenterWashington D.C.United States177
National Institutes of Health Clinical CenterBethesdaUnited States800
UPMC Children's Hospital of PittsburghPittsburghUnited States70