Rare Disease Trial, Recruiting

Written by an AI model from ClinicalTrials.gov eligibility criteria and checked on a sample basis. Please confirm against the original criteria.

Who might be able to join this trial:

• You have been diagnosed with primary hyperoxaluria (a rare genetic condition affecting how the body processes oxalate)
• You have been diagnosed with enteric hyperoxaluria (high oxalate levels in the urine caused by digestive system issues)
• You have been diagnosed with Dent Disease (a rare kidney condition affecting mostly males)
• You have been diagnosed with Cystinuria (a condition where too much of an amino acid called cystine builds up in the kidneys)
• You have been diagnosed with adenine phosphoribosyltransferase deficiency, also called APRTd (a rare inherited condition that can cause kidney stones)
• You have been diagnosed with Lowe Syndrome (a rare genetic condition affecting the eyes, brain, and kidneys)
• You have been identified as a carrier of Dent Disease (meaning you carry the gene for Dent Disease but may not have all the symptoms)

Who may not be able to join:

• You have previously experienced kidney failure
• You have had a liver transplant and/or a kidney transplant in the past

Important: Always verify eligibility with the trial site directly before applying.