methylmalonic acidemia
methylmalonic acidemia
Explore linked clinical trials. Standard reference: MONDO:00020128 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Clinical and Laboratory Study of Methylmalonic Acidemia | Congenital, 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 disorder | Recruiting | Not stated | 2026-10-08 | NCT00078078 | |
| A Prospective Study of Pediatric Participants up to 16 Years of Age With Methylmalonic Acidemia (MMA) Due to Mutations in the MMUT Gene | methylmalonic acidemia | Recruiting | Not stated | 2026-08-17 | NCT07432880 | |
| Long-term Follow-up Study of Patients Who Received hLB-001 Gene Therapy | methylmalonic acidemia | Active, not recruiting | Not stated | 2026-02-05 | NCT05506254 | |
| An Extension Study to Evaluate the Long-Term Safety and Clinical Activity of mRNA-3705 in Participants Previously Enrolled in Other Clinical Studies of mRNA-3705 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, inborn errors of metabolism, metabolic disease, methylmalonic acidemia | Recruiting | Phase 1 / Phase 2 | 2025-12-23 | NCT05295433 | |
| A Study to Evaluate the Effects and Safety of Hydroxocobalamin in Participants With Combined Methylmalonic Academia (cblC Type) | methylmalonic acidemia | Not yet recruiting | Phase 3 | 2025-09-09 | NCT07163364 | |
| An Observational Study of Carbaglu® for the Treatment of MMA and PA in Adults and Pediatrics | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hyperammonemia, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, hereditary disease, inborn disorder of amino acid metabolism, inborn errors of metabolism, metabolic disease, methylmalonic acidemia, propionic acidemia | Recruiting | Not stated | 2025-04-15 | NCT05040178 | |
| MyRareDiet A Novel Diet Tracking Tool | Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, brain disorder, central nervous system disorder, hereditary disease, inborn disorder of amino acid metabolism, inborn errors of metabolism, maple syrup urine disease, metabolic disease, methylmalonic acidemia, nervous system disorder, propionic acidemia, urea cycle disorder | Not yet recruiting | Not applicable | 2024-10-30 | NCT06664840 | |
| Understanding the Long-Term Management of Organic Acidemia Patients With CARBAGLU®: A Mixed Methods Approach | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, hereditary disease, inborn disorder of amino acid metabolism, inborn errors of metabolism, metabolic disease, methylmalonic acidemia, propionic acidemia | Recruiting | Not stated | 2024-02-05 | NCT04176523 |