Clinical Trial Update: Oxalate Excretion Profile in Patients with a Heterozygous Mutation of the AGXT (alanine-glyoxylate Aminotransferase) Gene [NA]

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Summary

A recruiting clinical trial studying oxalate excretion in patients with a heterozygous AGXT gene mutation, related to primary hyperoxaluria type 1.

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Diseases / indications

• Hyperoxaluria
• Hyperoxaluria Type

Snippet

Sponsor: Hospices Civils de Lyon | Conditions: Hyperoxaluria (Disorder) | NA | Status: RECRUITING