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COMPLETED
NCT06481150
PHASE4

A Novel Approach for Reducing Hyperoxaluria and Kidney Stone Risk.

Sponsor: University of Texas Southwestern Medical Center

View on ClinicalTrials.gov

Summary

This pilot study is proposing a novel approach to directly target intestinal oxalate absorption with the drug Tenapanor, which was recently FDA-approved for treating hyperphosphatemia in patients with chronic kidney disease. Tenapanor works by blocking paracellular phosphate absorption by the intestine, but the underlying mechanisms have not been clearly defined. Since phosphate and oxalate ions are absorbed through the same paracellular pathway, and are of similar size and charge, Tenapanor is hypothesized to also reduce dietary oxalate absorption and consequently lower urinary oxalate excretion.

Key Details

Gender

All

Age Range

18 Years - 99 Years

Study Type

INTERVENTIONAL

Enrollment

18

Start Date

2024-07-01

Completion Date

2025-09-14

Last Updated

2026-10-07

Healthy Volunteers

Yes

Conditions

Interventions

DRUG

Tenapanor

Each tablet 30 mg

OTHER

Placebo

Placebo

Locations (1)

UT Southwestern Medical Center

Dallas, Texas, United States