Primary Hyperoxaluria Type 2

Explore clinical trials studying Primary Hyperoxaluria Type 2. Study availability and eligibility vary by location and protocol.

3 public trials 0 recruiting studies

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Primary Hyperoxaluria Type 2 trial results

Not Yet Recruiting

NCT06465472

Conditions: Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, +16 more
Locations: Not specified

Completed

NCT05001269

Conditions: Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, +17 more
Locations: Clinical Research Site Rochester, Minnesota, United States

Clinical Research Site Hamilton, Ontario, Canada

Clinical Trial Site Bonn, Germany

Clinical Research Site Heidelberg, Germany

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Active, Not Recruiting

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