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Colchicine for Symptom and Inflammation in Knee Osteoarthritis

Information source: Singapore General Hospital
ClinicalTrials.gov processed this data on August 20, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Knee Osteoarthritis

Intervention: Colchicine (Drug); Placebo (Drug)

Phase: Phase 2/Phase 3

Status: Active, not recruiting

Sponsored by: Singapore General Hospital

Official(s) and/or principal investigator(s):
Ying Y Leung, MBChB, Principal Investigator, Affiliation: Singapore General Hospital
Virginia Kraus, MD, PhD, Principal Investigator, Affiliation: Duke University

Summary

Uric acid may be involved in the activation of the innate immune response in osteoarthritis (OA) pathology and progression. This suggests that traditional gout therapy may be beneficial for OA. Our goal therefore is to assess colchicine, an existing commercially available agent for gout, for a new therapeutic indication-knee OA. The investigators propose a randomized clinical trial (RCT) of 16 weeks' therapy with standard daily dose oral colchicine or placebo for knee OA. The investigators hypothesize that colchicine will block inflammasome mediated inflammation, thereby improve the signs and symptoms of OA, and reduce synovial fluid, serum and urine inflammatory and biochemical joint degradation biomarkers. This trial will potentially provide data to support a new treatment option for knee OA.

Clinical Details

Official title: A Randomized Controlled Trial of Colchicine for Symptom and Inflammation Modification in Knee Osteoarthritis

Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Primary outcome: 30% improvement in total Western Ontario and McMaster Universities Arthritis Index (WOMAC) of the signal knee.

Secondary outcome:

change in WOMAC pain score and physical function score

change in Health Assessment Questionnaire (HAQ)

change in quality of life

quantify of rescue medication used

Change in Synovitis and cartilage morphology on Magnetic Resonance Imaging

change in synovial fluid Interleukin-18, Interleukin-1β, or tumor necrosis factor -α

specific adverse event

OMERACT-ORSI response criteria

Detailed description: In a knee OA cohort with no clinical evidence or self-report of gout, The investigators recently found a significant correlation of synovial fluid uric acid with radiographic and scintigraphic measures of OA severity [1]. The investigators also observed strong correlations of OA severity (radiographically and scintigraphically determined) and synovial fluid uric acid with synovial fluid Interleukin (IL)-18 and IL-1β; these two cytokines are classically produced during gout attacks by innate immune system activation mediated by uric acid crystal-induced inflammasome assembly in macrophages. These results strongly support the involvement of uric acid and the innate immune system in OA pathology and progression. Whereas in gout flares, uric acid in a crystal form is what triggers the innate immune response, we suspect that in OA, uric acid in a microcrystalline or particulate form is the

pathogenic agent - - able to trigger an innate immune response; this leads to release of

inflammatory cytokines like IL-18, IL-1β and subsequently tumor necrosis factor - α which

perpetuates further cartilage degradation. This new conception of the pathogenesis of OA has very important treatment implications; it suggests that existing therapies for gout may be of benefit in OA. Colchicine may be an effective treatment for OA due to its capacity in suppressing the innate immune response at various levels. At micromolar concentrations colchicine suppresses activation of the crystal-induced (NACHT), (LRR) and (PYD) domains containing protein-3 (NALP3) inflammasome; IL-1β processing and release; and L-selectin expression on neutrophils [2]. At nanomolar concentrations colchicine has blocks the release of a crystal-derived chemotactic factor from neutrophil lysosomes; it blocks neutrophil adhesion to endothelium by modulating the distribution of adhesion molecules on the endothelial cells; and it inhibits urate crystal-induced production of superoxide anions from neutrophils and macrophages. The pain and symptom relieving effects of colchicine for knee OA have been demonstrated in three small but well-performed human randomized controlled trials [3-5]; however, the mechanism of action of colchicine in OA has never been evaluated. The investigators therefore propose a RCT of colchicine to examine the effects on signs and symptoms of knee OA and to evaluate the mechanism of action through analysis of synovial fluid and systemic biomarker profiles. Hypothesis: The investigators hypothesize that colchicine will block inflammasome mediated inflammation, thereby improve the signs and symptoms of OA, and reduce synovial fluid serum and urine inflammatory and biochemical joint degradation biomarkers. Aim 1. To determine whether daily oral colchicine at standard clinical doses (0. 5 mg two times daily), compared to placebo, can decrease the pain of symptomatic OA knee and improve function when used as adjunctive daily therapy in addition to background therapy with the patient's current stable analgesic regimen. Aim 2. To evaluate the mechanism of action of colchicine for reducing knee OA signs and

symptoms through analyses of synovial fluid, serum, and urine biomarker profiles - these

will interrogate and characterize the state of activation of joint metabolism (joint degradation and synthesis markers), inflammatory mediators, the innate immune system and the NALP3 inflammasome components specifically both before (at baseline) and after 16 weeks therapy (at study end) with oral colchicine versus placebo treatment. This pilot phase II study uses a double-blinded, randomized, placebo, controlled design. Patients with symptomatic and radiographic knee OA (n=120) will be randomized to colchicine (SIN 12490P) 0. 5 mg bid (n=60) or placebo (n=60) daily for 16 weeks. Patients will be permitted to remain on their baseline adjunctive therapy, including non-steroidal anti-inflammatory drugs (NSAIDs) without changes for the duration of the study. They will also be allowed the use of paracetamol not more than 2 g/day as rescue analgesia and pill counting at the end of the study will be conducted to determine the amount of rescue medicine utilized over the course of the 16-week study.

Eligibility

Minimum age: 21 Years. Maximum age: N/A. Gender(s): Both.

Criteria:

Inclusion Criteria:

- Symptomatic knee OA meeting American College of Rheumatology (ACR) criteria

- Radiographic criteria for knee OA with Kellgren-Lawrence (KL) stage of ≥ 2 in at

least one knee

- Response positive to the question "do you have pain, aching or stiffness of the knee

on most days of the past month

- Score of ≥ 40 out of 100 on a visual analogue scale (VAS) for pain

- Age ≥ 21 years or above

- Male and female subjects and all ethnicities included

- Patients to agree to avoid consuming grapefruit and grapefruit juice while using

colchicine

- Ability to provide informed consent

Exclusion Criteria:

- Exposure to a corticosteroid (either parenteral or oral) within 3 months prior to the

study enrolment

- Knee arthroscopic surgery within 6 months prior to the study enrolment

- Known history of avascular necrosis, inflammatory arthritis (e. g. Rheumatoid

Arthritis), Paget's disease, joint infection, periarticular fracture, neuropathic arthropathy, Reiter's syndrome, or gout involving the knee

- Contraindication to arthrocentesis (warfarin use, bleeding disorder, skin rash or

skin infection of signal knee)

- Knee joint replacement;

- History of podagra, active gout or treatment for gout

- Pregnancy or lactation - women of childbearing potential will have serum pregnancy

testing (ßHCG) at time of entry prior to any imaging studies (X-ray or MRI); female subjects of childbearing potential must agree to use some form of contraception during the 16 week trial and for 1 week after the end of the trial (over 6 half-life equivalents)

- Renal failure with serum creatinine > 150mmol/L (1. 7 mg/dL);

- Hepatic impairment defined by serum alanine transaminase (ALT) above the upper limit

of normal for the clinical laboratory performing the screening test

- Muscle impairment defined by elevated serum creatine phosphokinase (CPK) above the

upper limit of normal for the clinical laboratory performing the screening test

- Personnel directly affiliated with this study or their immediate family members

(defined as a spouse, parent, child or sibling, whether biological or legally adopted)

- Current enrolment in or discontinued within the last 30 days from a clinical trial

involving an off-label use of an investigational drug or device, or are concurrently enrolled in any other type of medical research judged to be scientifically or medically incompatible with this study

- Inability to understand and cooperate with the investigators or to give valid

consent;

- Contraindication for magnetic resonance imaging (MRI) - this is exclusion only for

the subset of individuals selected for this imaging procedure;

- Anticipation of need for joint replacement within 4 months of the start of the

intervention;

- Current treatment with drugs known to inhibit Cytochrome 450(3A4) isoforms and/or

P-glycoprotein (P-gp) that increase the risk of colchicine-induced toxic effects (see: http://www. fda. gov/Drugs/Drug-safety/PostmarketDrugSafetyInformationforPatientsandProviders/DrugSafetyInformationforHeathcareProfessionals/ucm174315. htm). Inclusion can be considered after 14 day wash out of agents listed in the drug information sheet, but only if treatment in the near future with one of these agents is not anticipated. The clinical necessity for such treatments during the study will require immediate discontinuation of the study drug and conversion of the patient to standard care. However, the patient will remain on study and scheduled measurements taken. Analyses will be performed on an intention-to-treat basis.

Locations and Contacts

Singapore General Hospital, Singapore 169608, Singapore
Additional Information

Starting date: October 2013
Last updated: June 18, 2015

Page last updated: August 20, 2015

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