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Alpha-Methylacyl-CoA Racemase Deficiency

Clinical trial condition

Alpha-Methylacyl-CoA Racemase Deficiency

Explore clinical trials studying Alpha-Methylacyl-CoA Racemase Deficiency. Study availability and eligibility vary by location and protocol.

2 public trials 1 recruiting study

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Alpha-Methylacyl-CoA Racemase Deficiency trial results

Recruiting

Longitudinal Natural History Study of Patients With Peroxisome Biogenesis Disorders (PBD)

NCT01668186

Conditions: ACBD5 (AcylCoA Binding Domain 5) Deficiency, ATP Binding Cassette Subfamily D Member 3 Gene Mutation, Abnormalities, Multiple, +48 more
Locations: Research Institute of the McGill University Health Center Montreal, Quebec, Canada

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Active, Not Recruiting

MT2013-31: Allo HCT for Metabolic Disorders and Severe Osteopetrosis

NCT02171104

Conditions: Abnormalities, Multiple, Acyl-CoA Oxidase Deficiency, Adrenoleukodystrophy With Cerebral Involvement, +85 more
Locations: Masonic Cancer Center, University of Minnesota Minneapolis, Minnesota, United States

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