Colchicine in Chronic Kidney Disease Patients

NCT ID: NCT06998862

Last Updated: 2025-05-31

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE3
• Total Enrollment: 744 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-02-12
• Study Completion Date: 2028-12-30

Brief Summary

The ColchiRen study is a phase 3, controlled, prospective, randomized, double-blind, and multicenter clinical trial. Its main objective is to demonstrate the benefit of low-dose colchicine treatment in secondary prevention of cardiovascular events in patients with moderate CKD. As a secondary objective, it aims to explore the potential beneficial anti-inflammatory effect on the progression of CKD.

Detailed Description

A total of 744 patients will be included (50% in each branch), and the follow-up time of the study will be three years.

EXPLORATORY PARAMETERS

• Analytical parameters in blood:

• Hemogram: hemoglobin, erythrocyte sedimentation rate.
• Biochemistry: creatinine, glomerular filtration rate estimated by CKD-EPI, glucose, triglycerides, total cholesterol, HDL-cholesterol, LDL-cholesterol, uric acid, C-reactive protein, fibrinogen, glycosylated hemoglobin.
• Analytical parameter in urine: albumin/creatinine ratio in first morning urine.
• Parameters in samples centralized in the Renal Pathophysiology Laboratory: array including more than 40 molecules that promote and inhibit inflammation and fibrosis; measurement of ACE and ACE2.
• Cardiovascular events defined as one of the following:

• Cardiovascular death.
• Acute coronary syndrome.
• Angina requiring hospitalization.
• Coronary revascularization.
• Transient ischemic attack or noncardioembolic ischemic stroke.
• Peripheral vascular disease, defined as acute peripheral arterial embolism or ischemia, or need for amputation or percutaneous surgical revascularization.
• Renal event, defined as one of the following:

• 40% decrease in glomerular filtration rate estimated by CKD-EPI with respect to baseline.
• Doubling of serum creatinine above baseline.
• Persistent drop in glomerular filtration rate estimated by CKD-EPI below 15 mL/min/1.73m2.
• Need for renal replacement therapy

Conditions

Chronic Kidney Disease; Cardiovascular Events

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: TRIPLE

Study Groups

Colchicine treatment

after randomization, a 0.5 mg tablet of colchicine per day will be administered.

Group Type: ACTIVE_COMPARATOR

colchicine treatment in chronic kidney disease patients

Intervention Type: DRUG

colchicine treatment 0.5 mg/day

placebo treatment

after randomization 0,25 mg of placebo per day will be administered

Group Type: PLACEBO_COMPARATOR

placebo treatment

Intervention Type: DRUG

placebo treatment 1 pill/day

Interventions

colchicine treatment in chronic kidney disease patients

colchicine treatment 0.5 mg/day

Intervention Type: DRUG

placebo treatment

placebo treatment 1 pill/day

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

Age between 18 and 99 years. Moderate chronic kidney disease, defined as an estimated glomerular filtration rate (eGFR) by the CKD-EPI formula between 30 and 59 mL/min/1.73 m².

History of a previous cardiovascular event:

Acute coronary syndrome. Admission for angina pectoris. Transient ischemic attack or non-cardioembolic ischemic stroke. Coronary revascularization. Peripheral vasculopathy, defined as: embolism or acute peripheral arterial ischemia, or the need for amputation or surgical revascularization.

Finding of coronary artery disease on imaging test.

Exclusion Criteria

• History of allergy or intolerance to colchicine or any of its excipients (dihydrate calcium hydrogen phosphate, microcrystalline cellulose, anhydrous colloidal silica, magnesium stearate).
• Current treatment with colchicine, or within the month prior to inclusion.
• Hospital admission for any cause within the 3 months prior to study inclusion.
• Active malignant neoplasm (except non-melanoma skin cancer or carcinoma in situ). Patients with a history of malignant neoplasm who have remained disease-free for the past 3 years may be included.
• Uncontrolled or symptomatic chronic inflammatory disease (rheumatoid arthritis, systemic lupus erythematosus, Crohn's disease, ulcerative colitis, etc.).
• Active infection with hepatitis B virus, hepatitis C virus, or human immunodeficiency virus.
• Liver cirrhosis of any cause, grade B or C according to Child-Pugh.
• Immunosuppressive treatment within the 12 weeks prior to study inclusion.
• Chronic treatment with non-steroidal anti-inflammatory drugs (NSAIDs).
• Poorly controlled hypertension (>160/90 mmHg) at the time of inclusion.
• Pregnancy and breastfeeding at the time of inclusion. Contraceptive methods are required for women of reproductive age. Women with no capacity for pregnancy are considered to be those with:

History of hysterectomy, bilateral salpingectomy, bilateral oophorectomy, or bilateral tubal ligation.

Documented infertility. Postmenopausal women, defined as amenorrhea for more than 12 months without other medical cause. In case of doubt, confirmation with elevated follicle-stimulating hormone (FSH) levels is recommended.

Women of reproductive capacity must use a method of contraception with proven effectiveness until 8 weeks after the end of the study. Acceptable methods include:

Intrauterine device (IUD) placement at least 6 weeks before study inclusion. Hormonal contraception with progestogens only, associated with ovulation inhibition: oral, injectable, or implantable, at least 6 weeks before study inclusion.

Progestin-releasing intrauterine system (IUS) at least 6 weeks before study inclusion.

Combined hormonal contraception (containing estrogen and progestogens) associated with ovulation inhibition: oral, intravaginal, transdermal, at least 6 weeks before study inclusion.

Other contraceptive methods (sexual abstinence, barrier methods, spermicides, etc.) are not considered acceptable for participation in this study

• Gastric ulcer
• thrombocytopenia <50,000 cells/μL during the month prior to inclusion
• Neutropenia defined as <1500 cells/mcL during the month prior to inclusion.
• Anemia defined as hemoglobin <10.5 g/dL during the month prior to inclusion.
• History of aplastic anemia diagnosed through bone marrow biopsy.
• Treatment with CYP3A4 inhibitors and/or P-glycoprotein inhibitors (antivirals, azole antifungals, aminoglycosides, cyclosporine) in the month prior to their inclusion in the study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 99 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Hospital General Universitario Gregorio Marañon

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Hospital General Universitario Gregorio Marañon

Madrid, Madrid, Spain

Site Status: RECRUITING

Countries

Spain

Facility Contacts

Marian Goicoechea, Md, PhD

Role: primary

marian.goicoechea@gmail.com

0034609838684

Other Identifiers

2023-505868-11-00

Identifier Type: CTIS

Identifier Source: secondary_id

FIBHGM-ECNC002-2022

Identifier Type: -

Identifier Source: org_study_id