Targeted Dose Finding of Canakinumab (ACZ885) for Management of Acute Flare in Refractory or Contraindicated Gout Patients

This study has been completed.
Sponsor:
Information provided by:
Novartis
ClinicalTrials.gov Identifier:
NCT00798369
First received: November 25, 2008
Last updated: April 9, 2012
Last verified: April 2012
  Purpose

This 8-week study is designed to determine the target dose of canakinumab (ACZ885) for the management of acute flare in gout patients who are contraindicated to Non-Steroidal anti-inflammatory drugs and/or colchicine. The efficacy of ACZ885 will be compared to the corticosteroid triamcinolone acetonide.


Condition Intervention Phase
Acute Gout
Drug: Canakinumab
Drug: Triamcinolone acetonide
Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
Official Title: An Adaptive Dose-ranging, Multi-center, Single-blind, Double-dummy, Active-controlled Trial to Determine the Target Dose of Canakinumab (ACZ885) in the Treatment of Acute Flares in Gout Patients Who Are Refractory or Contraindicated to NSAIDs and/or Colchicine

Resource links provided by NLM:


Further study details as provided by Novartis:

Primary Outcome Measures:
  • The Dose of Canakinumab for Treatment of Acute Flares in Gout Patients That Leads to the Same Efficacy as Triamcinolone Acetonide With Respect to Pain Intensity on a 0-100 mm Visual Analog Scale (VAS) [ Time Frame: at 24,48 and 72 hours post-baseline ] [ Designated as safety issue: No ]
    Mean target dose at 24, 48 and 72 hours. Four models: Emax, Logistic, Linear in log-dose, Linear were selected to describe the potential dose-response curve and hence estimate the target dose of canakinumab using baseline Visual Analog Scale (VAS) and Body Mass Index (BMI) as covariates. Target dose was defined as the dose for which the efficacy is equivalent to the efficacy of triamcinolone acetonide 40 mg and was identified by assessing the dose response relationship with regards to the pain intensity in the target joint measured on a 0- 100 mm VAS (0= no pain and 100= unbearable pain).


Secondary Outcome Measures:
  • The Change in Pain Intensity in the Target Joint Following Canakinumab Administration Compared to Triamcinolone Acetonide [ Time Frame: Baseline,at 72 hrs post-dose and 7 days post-dose ] [ Designated as safety issue: No ]
    The change in pain intensity from baseline to 72 hours and 7 days post dose as measured on a 0-100 mm Visual Analog Scale(VAS): 0= no pain and 100= severe pain. Analysis of Covariance (ANCOVA) with treatment group, VAS at baseline and Body mass Index (BMI) at baseline as covariates. Change from baseline = (post-baseline measurement - baseline).

  • Percentage of Participants With an Excellent or Good Response With Regards to the Patient's Global Assessment of Response to Treatment [ Time Frame: at 72 hours post-baseline ] [ Designated as safety issue: No ]
    Participants scored their global assessment of response to treatment using a 5-point Likert scale: Excellent, Good, Acceptable, Slight and Poor.

  • The Time to 50% Reduction of Baseline Pain Intensity in the Target Joint [ Time Frame: Baseline, within 7 days after randomization ] [ Designated as safety issue: No ]
    The median time in days to at least 50% reduction in Pain intensity from baseline as measured by Visual Analog Scale (VAS) for each treatment group. Participants scored their pain intensity in the target joint on a 0-100 mm VAS, ranging from no pain (0) to unbearable pain (100).

  • High Sensitivity C-reactive Protein (hsCRP) at 72 Hours, 7days, 4 Weeks and 8 Weeks Post Dose for Each Treatment Group [ Time Frame: at 72 hours and 7 days, 4 and 8 weeks post-dose ] [ Designated as safety issue: No ]

    High sensitivity C-reactive protein (hsCRP) was determined in serum at all visits (Visits 1-5) in order to identify the presence of inflammation, to determine its severity, and to monitor response to treatment.

    ANCOVA with treatment group, protein level at baseline and BMI at baseline as covariates.


  • Serum Amyloid Protein (SAA) Levels at 72 Hours, 7days, 4 Weeks and 8 Weeks Post Dose for Each Treatment Group [ Time Frame: at 72 hours and 7 days, 4 and 8 weeks post-dose ] [ Designated as safety issue: No ]

    Serum amyloid A (SAA) were determined in serum at all visits (Visits 1-5) in order to identify the presence of inflammation, to determine its severity, and to monitor response to treatment.

    ANCOVA with treatment group, protein level at baseline and BMI at baseline as covariates.


  • Amount of Rescue Medication Taken for Each Treatment Group [ Time Frame: 7 days after study drug administration ] [ Designated as safety issue: No ]
    Participants who had difficulty in tolerating their pain after the 6-hour post-dose pain assessments and during the first 7 study days were allowed to take a maximum of 30 mg prednisolone (or equivalent dose of prednisone [30 mg]) orally once a day for a maximum of 5 days. In addition, participants could use 500 mg acetaminophen (paracetamol) and/or 30 mg codeine as needed during the first 7 study days. A maximum of 1 g/dose or 3 g/day of acetaminophen and 30 mg/dose or 180 mg/day of codeine was allowed during the first 7 days of the study.


Enrollment: 200
Study Start Date: November 2008
Study Completion Date: August 2009
Primary Completion Date: August 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Canakinumab 10 mg
Canakinumab 10 mg subcutaneous (s.c) once. The s.c. injection could be administered into the arm or thigh. Randomized patients received one s.c. injection of canakinumab and placebo matching triamcinolone acetonide (0.9% sodium chloride) intramuscularly (i.m.) once, on Day 1. The i.m. injection was recommended to be administered deeply into the gluteal muscle.
Drug: Canakinumab
Randomized patients received one s.c. injection of canakinumab and placebo matching triamcinolone acetonide (0.9% sodium chloride) intramuscularly (i.m.) once, on Day 1. The i.m. injection was recommended to be administered deeply into the gluteal muscle.
Experimental: Canakinumab 25 mg
Canakinumab 25 mg subcutaneous (s.c) once. The s.c. injection could be administered into the arm or thigh. Randomized patients received one s.c. injection of canakinumab and placebo matching triamcinolone acetonide (0.9% sodium chloride) intramuscularly (i.m.) once, on Day 1. The i.m. injection was recommended to be administered deeply into the gluteal muscle.
Drug: Canakinumab
Randomized patients received one s.c. injection of canakinumab and placebo matching triamcinolone acetonide (0.9% sodium chloride) intramuscularly (i.m.) once, on Day 1.
Experimental: Canakinumab 50 mg
Canakinumab 50 mg subcutaneous (s.c) once. The s.c. injection could be administered into the arm or thigh. Randomized patients received one s.c. injection of canakinumab and placebo matching triamcinolone acetonide (0.9% sodium chloride) intramuscularly (i.m.) once, on Day 1. The i.m. injection was recommended to be administered deeply into the gluteal muscle.
Drug: Canakinumab
Randomized patients received one s.c. injection of canakinumab and placebo matching triamcinolone acetonide (0.9% sodium chloride) intramuscularly (i.m.) once, on Day 1.
Experimental: Canakinumab 90 mg
Canakinumab 90 mg subcutaneous (s.c) once. The s.c. injection could be administered into the arm or thigh. Randomized patients received one s.c. injection of canakinumab and placebo matching triamcinolone acetonide (0.9% sodium chloride) intramuscularly (i.m.) once, on Day 1. The i.m. injection was recommended to be administered deeply into the gluteal muscle.
Drug: Canakinumab
Randomized patients received one s.c. injection of canakinumab and placebo matching triamcinolone acetonide (0.9% sodium chloride) intramuscularly (i.m.) once, on Day 1.
Experimental: Canakinumab 150 mg
Canakinumab 150 mg subcutaneous (s.c) once. The s.c. injection could be administered into the arm or thigh. Randomized patients received one s.c. injection of canakinumab and placebo matching triamcinolone acetonide (0.9% sodium chloride) intramuscularly (i.m.) once, on Day 1. The i.m. injection was recommended to be administered deeply into the gluteal muscle.
Drug: Canakinumab
Randomized patients received one s.c. injection of canakinumab and placebo matching triamcinolone acetonide (0.9% sodium chloride) intramuscularly (i.m.) once, on Day 1.
Active Comparator: Triamcinolone acetonide 40 mg
Triamcinolone acetonide 40 mg intramuscularly (i.m) once. The i.m. injection was recommended to be administered deeply into the gluteal muscle. Randomized patients received triamcinolone acetonide 40 mg i.m. once and placebo matching canakinumab s.c. once, on Day 1.
Drug: Triamcinolone acetonide
Randomized patients received triamcinolone acetonide 40 mg i.m. once and placebo matching canakinumab s.c. once, on Day 1.

  Eligibility

Ages Eligible for Study:   18 Years to 80 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • History of at least 1 gout flare prior to the Screening Visit
  • Meeting the American College of Rheumatology (ACR) 1977 preliminary criteria for the classification of acute arthritis of primary gout.
  • Presence of acute gout flare for no longer than 5 days.
  • Baseline pain intensity > or = to 50 mm on the 0-100 mm VAS.
  • Contraindicated for, intolerant or unresponsive to NSAIDs, colchicine or both.

Exclusion Criteria:

  • Rheumatoid arthritis, evidence/suspicion of infectious/septic arthritis, or other acute inflammatory arthritis.
  • Presence of severe renal function impairment
  • Contraindication to intramuscular injection
  • Known presence or suspicion of active or recurrent bacterial, fungal or viral infection at the time of enrollment
  • Evidence of active pulmonary disease
  • Live vaccinations within 3 months prior to the start of the study
  • Use of forbidden therapy

Other protocol-defined inclusion/exclusion criteria applied

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00798369

  Hide Study Locations
Locations
United States, Alabama
Pinnacle Research Group, LLC
Anniston, Alabama, United States, 36207-5710
University of Alabama at Birmingham
Birmingham, Alabama, United States, 35294
United States, California
Associated Pharmaceutical Research
Buena Park, California, United States, 90620
Northern California Institute for Bone Health
Oakland, California, United States, 94609
San Diego Arthritis & Osteoporosis Medical Clinic
San Diego, California, United States, 92108
Center for Clinical Trials of San Gabriel
West Covina, California, United States, 91790
United States, Florida
Tampa Medical Group, P.A.
Tampa, Florida, United States, 33614
Florida Medical Clinic, PA
Zephyrhills, Florida, United States, 33542
United States, Georgia
Harbin Clinic
Rome, Georgia, United States, 30165
United States, Idaho
Intermountain Orthopedics
Boise, Idaho, United States, 83702
Northwest Clinical Trials
Boise, Idaho, United States, 83704
United States, Illinois
The Arthritis Center
Springfield, Illinois, United States, 62704
United States, Kansas
Cotton O'Neil Clinic
Topeka, Kansas, United States, 66606
United States, Louisiana
Arthritis and Diabetes Clinic
Monroe, Louisiana, United States, 71203
United States, Missouri
Arthritis Consultants, Inc.
St. Louis, Missouri, United States, 63141
United States, Montana
Billings Clinic Research Center
Billings, Montana, United States, 59101
Montana Medical Research
Missoula, Montana, United States, 59804
United States, Nebraska
Heartland Clinical Research, Inc.
Omaha, Nebraska, United States, 68134
United States, New Mexico
New Mexico Clinical Research & Osteoporosis Center, Inc.
Albuquerque, New Mexico, United States, 87106
United States, New York
Regional Clinical Research Rheumatology Assoc.
Binghamton, New York, United States, 13905
United States, Pennsylvania
Altoona Center for Clinical Research
Duncansville, Pennsylvania, United States, 16635
United States, South Carolina
Community Research Partners, Inc.
Varnville, South Carolina, United States, 29944
United States, Tennessee
Comprehensive Rheumatology
Hendersonville, Tennessee, United States, 37075
MultiSpecialty Clinical Research
Johnson City, Tennessee, United States, 37601
Integrity Clinical Research, LLC
Milan, Tennessee, United States, 38358
United States, Texas
Southwest Rheumatology
Mesquite, Texas, United States, 75150
United States, Virginia
Health Research of Hampton Roads
Newport News, Virginia, United States, 23606
Argentina
Novartis Investigative site
Rosario, Argentina
Belgium
Novartis Investigative site
Gozée, Belgium
Canada
Novartis Investigative site
Moncton, Canada
Novartis Investigative site
Mount Pearl, Canada
Novartis Investigative site
St. John's, Canada
France
Novartis Investigative site
Paris cedex 10, France
Germany
Novartis Investigative Site
Bad Nauheim, Germany
Novartis Investigative Site
Bautzen, Germany
Novartis Investigative Site
Berlin, Germany
Novartis Investigative Site
Chemnitz, Germany
Novartis Investigative Site
Dachau, Germany
Novartis Investigative Site
Dresden, Germany
Novartis Investigative Site
Frankfurt, Germany
Novartis Investigative Site
Georgensgmuend, Germany
Novartis Investigative Site
Hamburg, Germany
Novartis Investigative Site
Leipzig, Germany
Novartis Investigative Site
Loehne, Germany
Novartis Investigative Site
Magdeburg, Germany
Novartis Investigative Site
Messkirch, Germany
Novartis Investigative Site
Munich, Germany
Novartis Investigative Site
Schwabach, Germany
Novartis Investigative Site
Zerbst, Germany
Poland
Novartis Investigative site
Poznan, Poland
Novartis Investigative site
Szczecin, Poland
Novartis Investigative site
Wroclaw, Poland
Russian Federation
Novartis Investigative site
Chelyabinsk, Russian Federation
Novartis Investigative Site
Moscow, Russian Federation
Novartis Investigative Site
St. Petersburg, Russian Federation
Novartis Investigative site
Tyumen, Russian Federation
Novartis Investigative Site
Yaroslavl, Russian Federation
Novartis Investigative site
Yekaterinburg, Russian Federation
Switzerland
Novartis Investigative site
Baden, Switzerland
Novartis Investigative site
Basel, Switzerland
Novartis Investigative site
Bern, Switzerland
Novartis Investigative site
Lausanne, Switzerland
Turkey
Novartis Investigative Site
Adana, Turkey
Novartis Investigative Site
Ankara, Turkey
Novartis Investigative Site
Antalya, Turkey
Novartis Investigative Site
Aydin, Turkey
Novartis Investigative Site
Gaziantep, Turkey
Novartis Investigative Site
Istanbul, Turkey
Novartis Investigative Site
Izmir, Turkey
Novartis Investigative Site
Manisa, Turkey
Novartis Investigative site
Sihhiye/Ankara, Turkey
United Kingdom
Novartis Investigative Site
Antrim, United Kingdom
Novartis Investigative Site
Coventry, United Kingdom
Novartis Investigative Site
Lancashire, United Kingdom
Novartis Investigative Site
Wellingborough, United Kingdom
Sponsors and Collaborators
Novartis
  More Information

No publications provided by Novartis

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: External Affairs, Novartis Pharmaceuticals
ClinicalTrials.gov Identifier: NCT00798369     History of Changes
Other Study ID Numbers: CACZ885H2255, EudraCT 2008-004666-61
Study First Received: November 25, 2008
Results First Received: January 20, 2011
Last Updated: April 9, 2012
Health Authority: Argentina: Ministry of Health
Belgium: Federal Agency for Medicinal Products and Health Products
Canada: Health Canada
France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Germany: Federal Institute for Drugs and Medical Devices
Poland: Office for Registration of Medicinal Products, Medical Devices and Biocidal Products
Russia: Pharmacological Committee, Ministry of Health
Switzerland: Federal Office of Public Health
Turkey: Ministry of Health
United Kingdom: Medicines and Healthcare Products Regulatory Agency
United States: Food and Drug Administration

Keywords provided by Novartis:
Acute flares
Gout
Anti-interleukin-1β monoclonal antibody
Colchicine
Triamcinolone acetonide

Additional relevant MeSH terms:
Gout
Arthritis
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases
Purine-Pyrimidine Metabolism, Inborn Errors
Metabolism, Inborn Errors
Genetic Diseases, Inborn
Metabolic Diseases
Antibodies, Monoclonal
Triamcinolone Acetonide
Colchicine
Triamcinolone hexacetonide
Triamcinolone
Triamcinolone diacetate
Immunologic Factors
Physiological Effects of Drugs
Pharmacologic Actions
Gout Suppressants
Antirheumatic Agents
Therapeutic Uses
Tubulin Modulators
Antimitotic Agents
Mitosis Modulators
Molecular Mechanisms of Pharmacological Action
Antineoplastic Agents
Anti-Inflammatory Agents
Glucocorticoids
Hormones
Hormones, Hormone Substitutes, and Hormone Antagonists

ClinicalTrials.gov processed this record on August 28, 2014