The primary purpose of this study is to evaluate the effect of lumasiran on the percent change in urinary oxalate excretion in patients with recurrent calcium oxalate kidney stone disease.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
2
Percent Change in 24-hour Urinary Oxalate From Baseline to Month 6
Time frame: Baseline to Month 6
Percentage of Patients Who Achieve a ≥20% Reduction in 24-hour Urinary Oxalate From Baseline to Month 6
Time frame: Baseline to Month 6
Percent Change in Urinary Calcium Oxalate Supersaturation From Baseline to Month 6
Time frame: Baseline to Month 6
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Clinical Trial Site
Birmingham, Alabama, United States
Clinical Trial Site
Northridge, California, United States
Clinical Trial Site
San Francisco, California, United States
Clinical Trial Site
Hialeah, Florida, United States
Clinical Trial Site
Acworth, Georgia, United States
Clinical Trial Site
Quincy, Illinois, United States
Clinical Trial Site
Carmel, Indiana, United States
Clinical Trial Site
Boston, Massachusetts, United States
Clinical Trial Site
Edina, Minnesota, United States
Clinical Trial Site
Rochester, Minnesota, United States
...and 21 more locations