Inflammation REduction to Prevent cArdiovascular Injury in Renal Disease (REPAIR)

Overview

Phase 1 basket trial including 2 open-label single-arm cohorts: REPAIR CKD cohort and REPAIR Dialysis cohort. Open label colchicine 0.3 mg daily for 8 weeks followed, in patients who tolerated the 0.3 mg dose, by forced titration to 0.6 mg daily for 8 weeks.

Detailed description

The REPAIR CKD cohort will enroll 100 patients with chronic kidney disease not requiring dialysis. The REPAIR Dialysis cohort will enroll 100 patients with chronic kidney disease requiring chronic maintenance dialysis. Each participant will be followed for up to 17 weeks, to determine among adults with severe chronic kidney disease not requiring dialysis and (separately) in those requiring dialysis, the proportion who, over 8 weeks of treatment, discontinue colchicine 1) 0.3 mg daily and 2) 0.6 mg daily.

Interventions

• Drug Colchicine
  0.3mg and 0.6mg tablets

Primary outcome measures

• Dose tolerance [Time frame: Up to 17 weeks]
• Early discontinuations [Time frame: Up to 17 weeks]

Secondary outcome measures (3)

• Reason for drug discontinuation [Time frame: Up to 17 weeks]
• Drug adherence [Time frame: Up to 17 weeks]
• Major Side Effects [Time frame: Up to 17 weeks]

Eligibility criteria

Inclusion criteria

• One of either:

1.2 Estimated GFR using CKD-EPI 2021 equation of ≤30 ml/min/1.73m2 on at least two occasions separated by at least 2 months and do not yet require dialysis and are not expected by their treating nephrologist to require dialysis in the next 6 months (REPAIR CKD cohort), or 1.3 receiving chronic maintenance dialysis 2 or more times per week for the previous 90 days (REPAIR Dialysis cohort);

• Age ≥18 years
• Provide informed consent to participate.

Exclusion criteria

• Currently treated with and cannot withdraw colchicine due to medical necessity; or
• Known allergy/sensitivity to colchicine; or
• Prior self-reported intolerance to colchicine at a dose of 0.6 mg daily or lower; or
• Currently pregnant or planning to become pregnant or breastfeed during the study; or
• Of childbearing potential AND do not have a negative pregnancy test OR do not agree to use two forms of contraception for the duration of the study; or
• Anticipated living donor renal transplant within the next 6 months; or
• Using a strong inhibitor of p-glycoprotein or strong inhibitor of CYP3A4 in the last 14 days; or
• B12 deficiency not managed with intramuscular supplementation; or
• Uncontrolled chronic diarrhea; or
• Cirrhosis, or chronic active hepatitis; or
• Pre-existent neuromuscular disease or persistent serum CK level > 3 times the upper limit of normal as measured within the past 60 days and determined to be non-transient through repeat testing; or
• Patient with any of the following within the past 60 days:

• white blood cell count < 3.0 X 109/L; or
• platelet count <110 X 109/L; or
• ALT or AST > 3 times the upper limit of normal (ULN); or
• total bilirubin > 2 times ULN and not due to Gilbert syndrome.
• Patient is considered by the investigator, for any reason, to be an unsuitable candidate for the study.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Non-randomized

Model

Parallel assignment

Masking

Open label

Primary purpose

Prevention

Study locations

Canada · 3 centers

• University of Alberta Hospital — Edmonton
• St. Joseph's Healthcare Hamilton — Hamilton
• London Health Sciences Centre — London

Identifiers

NCT: NCT06203977 · REPAIR

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗