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Terminated Phase 2 Interventional Results available

A Study to Evaluate Lumasiran in Adults With Recurrent Calcium Oxalate Kidney Stone Disease and Elevated Urinary Oxalate Levels

ClinicalTrials.gov ID: NCT05161936

Public ClinicalTrials.gov record NCT05161936. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 24, 2026, 9:04 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy, Safety, Pharmacodynamics, and Pharmacokinetics of Lumasiran in Patients With Recurrent Calcium Oxalate Kidney Stone Disease and Elevated Urinary Oxalate Levels

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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 identification

NCT ID
NCT05161936
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Alnylam Pharmaceuticals
Industry
Enrollment
2 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 27, 2022 (Actual)
Primary completion
Nov 1, 2022 (Actual)
Completion
Nov 1, 2022 (Actual)
Last update posted
May 22, 2024

2022

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
Clinical Trial Site Birmingham Alabama 35233 —
Clinical Trial Site Northridge California 91324 —
Clinical Trial Site San Francisco California 94143 —
Clinical Trial Site Hialeah Florida 33016 —
Clinical Trial Site Acworth Georgia 30101 —
Clinical Trial Site Quincy Illinois 62301 —
Clinical Trial Site Carmel Indiana 46032 —
Clinical Trial Site Boston Massachusetts 02114 —
Clinical Trial Site Edina Minnesota 55435 —
Clinical Trial Site Rochester Minnesota 55905 —
Clinical Trial Site Las Vegas Nevada 89128 —
Clinical Trial Site Albany New York 12208 —
Clinical Trial Site Garden City New York 11530 —
Clinical Trial Site Greensboro North Carolina 27403 —
Clinical Trial Site North Charleston South Carolina 29405 —
Clinical Trial Site El Paso Texas 79902 —
Clinical Trial Site Houston Texas 77054 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 14 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05161936, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 22, 2024 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05161936 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →