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Hereditary renal hypouricemia
MONDO:0009071Hereditary renal hypouricemia (HRH) is a rare autosomal recessively inherited renal membrane transport disorder affecting urate reabsorption in the proximal tubules leading to usually asymptomatic hypouricemia and predisposing to urolithiasis and exercise induced acute renal failure (EIARF).
Also known as: Dalmatian hypouricemia, hypouricemia, renal, renal hypouricemia
3 clinical trials for this condition and its sub-types, 2 tagged with Hereditary renal hypouricemia itself.
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Browse by category →Sub-types of Hereditary renal hypouricemia
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Hypouricemia, renal 1 trial · 2 incl. sub-types
2 sub-types
- Hypouricemia, renal 1 1 trial
- Hypouricemia, renal, 2 0 trials
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New pill aims to tame high uric acid in kidney patients
Disease control Recruiting nowThis study tests an experimental drug called IG3018 for people with high uric acid, some of whom also have chronic kidney disease. About 60 adults will receive either the drug or a placebo for 4 weeks. Researchers will check safety, side effects, and how well the drug lowers uric…
Phase 1/2 • Sponsor: Intelligem Therapeutics Australia Pty Ltd. • Aim: Disease control
Last updated Jun 27, 2026 09:01 UTC
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Scientists launch major study to unravel mysterious metabolism disorders
Knowledge-focused Recruiting nowThis study aims to learn more about rare disorders that affect how the body processes chemicals called pyrimidines and purines. These disorders can cause problems in the brain, blood, kidneys, and immune system, ranging from mild to life-threatening. Researchers will compare test…
Sponsor: National Human Genome Research Institute (NHGRI) • Aim: Knowledge-focused
Last updated Aug 21, 2026 00:00 UTC