ClinicalTrials.gov record
Completed Phase 2 Interventional

A Study to Evaluate TOUR006 in Patients With Chronic Kidney Disease and Elevated Hs-CRP

ClinicalTrials.gov ID: NCT06362759

Public ClinicalTrials.gov record NCT06362759. 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 May 20, 2026, 10:02 AM 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 Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Quarterly and Monthly TOUR006 in Participants With Chronic Kidney Disease and Elevated High-Sensitivity C-Reactive Protein

Study identification

NCT ID
NCT06362759
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Tourmaline Bio, Inc.
Industry
Enrollment
143 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
May 14, 2024
Primary completion
Mar 5, 2025
Completion
Dec 3, 2025
Last update posted
Feb 23, 2026

2024 – 2025

United States locations

U.S. sites
38
U.S. states
22
U.S. cities
35
Facility City State ZIP Site status
Site - 0101 Birmingham Alabama 35209
Site - 0135 Huntsville Alabama 35763
Site - 0145 Huntsville Alabama 35805
Site - 0104 Phoenix Arizona 85018
Site - 0125 San Dimas California 91773
Site - 0112 Valencia California 91355
Site - 0128 Valencia California 91355
Site - 0136 Stamford Connecticut 06905
Site - 0113 Greenacres City Florida 334667
Site - 0149 Pembroke Pines Florida 33024
Site - 0144 Plantation Florida 33317
Site - 0119 Port Orange Florida 32127
Site - 0151 Tampa Florida 33634
Site - 0122 Savannah Georgia 31406
Site - 0106 Chicago Illinois 60655
Site - 0115 Morton Illinois 61550
Site - 0114 Council Bluffs Iowa 51501
Site - 0129 Metairie Louisiana 70006
Site - 0123 Las Vegas Nevada 89121
Site - 0130 Middletown New York 10940
Site - 0110 Charlotte North Carolina 28208
Site - 0117 Fargo North Dakota 58104
Site - 0120 Cincinnati Ohio 45219
Site - 0127 Marion Ohio 43302
Site - 0132 Bethlehem Pennsylvania 18017
Site - 0126 Providence Rhode Island 02818
Site - 0102 Fort Mill South Carolina 29707
Site - 0103 Greenville South Carolina 29607
Site - 0108 Knoxville Tennessee 37923
Site - 0148 Greenville Texas 75402
Site - 0105 Houston Texas 77043
Site - 0111 Lampasas Texas 76550
Site - 0150 McKinney Texas 75069
Site - 0107 San Antonio Texas 78212
Site - 0141 San Antonio Texas 78255
Site - 0109 Manassas Virginia 20110
Site - 0147 Morgantown West Virginia 26505
Site - 0134 Kenosha Wisconsin 53144

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06362759, 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 Feb 23, 2026 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06362759 live on ClinicalTrials.gov.

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