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Methylmalonic acidemia with homocystinuria

Clinical trial condition

Methylmalonic acidemia with homocystinuria

Explore clinical trials studying Methylmalonic acidemia with homocystinuria. Study availability and eligibility vary by location and protocol.

3 public trials 1 recruiting study

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Methylmalonic acidemia with homocystinuria trial results

Recruiting

Longitudinal Study of Ultra-rare Inherited Metabolic and Degenerative Neurological Diseases.

NCT04880356

Conditions: 2-Hydroxyglutaricaciduria, Adrenal Gland Diseases, Adrenal Insufficiency, +58 more
Locations: Fondazione IRCCS Istituto Neurologico Carlo Besta Milan, Milano, Italy

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Completed

EPI-743 in Cobalamin C Defect: Effects on Visual and Neurological Impairment

NCT01793090

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Genetic Disease, +5 more
Locations: Bambino Gesù Hospital and Research Institute Rome, Italy

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Active, Not Recruiting

Early Check: Expanded Screening in Newborns

NCT03655223

Conditions: 17 Alpha-Hydroxylase Deficiency, 3-Hydroxy-3-Methylglutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, +456 more
Locations: RTI International Research Triangle Park, North Carolina, United States

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