5 studies found for: "pyruvate carboxylase deficiency" OR "Pyruvate Metabolism, Inborn Errors"
Compassionate Use of Triheptanoin (C7) for Fatty Acid Oxidation Disorders and Glycogen Storage Disease
Pyruvate Kinase Deficiency Natural History Study
Open-Label, Dose-Escalating Study to Assess Safety, Tolerability, Efficacy, PK and PD of RP103 in Children With Inherited Mitochondrial Disease
Tissue Sample Study for Mitochondrial Disorders
|5||Active, not recruiting||
Safety and Efficacy Study of EPI-743 in Children With Leigh Syndrome
† Indicates status has not been verified in more than two years