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Cardiovascular Safety of Febuxostat and Allopurinol in Patients With Gout and Cardiovascular Comorbidities (CARES)

This study is currently recruiting participants.
Verified January 2013 by Takeda Global Research & Development Center, Inc.
Sponsor:
Information provided by (Responsible Party):
Takeda Global Research & Development Center, Inc.
ClinicalTrials.gov Identifier:
NCT01101035
First received: April 7, 2010
Last updated: January 17, 2013
Last verified: January 2013
History of Changes
  Purpose

The purpose of this study is to see if subjects with gout who receive febuxostat or allopurinol, once daily (QD), have a higher rate of serious heart and blood vessel complications.


Condition Intervention Phase
Cardiovascular Disease
 Drug: Febuxostat
Drug: Allopurinol
 Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Multicenter, Randomized, Active-Control, Phase 3B Study to Evaluate the Cardiovascular Safety of Febuxostat and Allopurinol in Subjects With Gout and Cardiovascular Comorbidities

Resource links provided by NLM:

MedlinePlus related topics: Gout Heart Attack
U.S. FDA Resources

Further study details as provided by Takeda Global Research & Development Center, Inc.:

Primary Outcome Measures:
  • First occurrence of any event in the predefined Major Adverse Cardiovascular Events Composite. [ Time Frame: At first occurrence (up to 60 Months) ] [ Designated as safety issue: Yes ]
    The time from randomization to the first occurrence of any event in the predefined Major Adverse Cardiovascular Events (MACE) Composite, which includes: Cardiovascular death, Non-fatal Myocardial Infarction, Nonfatal Stroke and Unstable Angina with Urgent Coronary Revascularization.


Secondary Outcome Measures:
  • First occurrence of any Antiplatelet Trialists' Collaborative Event. [ Time Frame: At first occurrence (up to 60 Months) ] [ Designated as safety issue: Yes ]
    The time from randomization to the first occurrence of any Antiplatelet Trialists' Collaborative Event, which includes Cardiovascular Death, Non-fatal Myocardial Infarction or Non-fatal Stroke.

  • First occurrence of Cardiovascular Death death. [ Time Frame: At first occurrence (up to 60 Months) ] [ Designated as safety issue: Yes ]
    The time from randomization to the first occurrence of Cardiovascular Death.

  • First occurrence of Non-fatal Myocardial Infarction. [ Time Frame: At first occurrence (up to 60 Months) ] [ Designated as safety issue: Yes ]
    The time from randomization to the first occurrence of nonfatal Myocardial Infarction.

  • First occurrence of Non-fatal stroke. [ Time Frame: At first occurrence (up to 60 Months) ] [ Designated as safety issue: Yes ]
    The time from randomization to the first occurrence of Non-fatal Stroke.

  • First occurrence of Unstable Angina with Urgent Coronary Revascularization. [ Time Frame: At first occurrence (up to 60 Months) ] [ Designated as safety issue: Yes ]
    The time from randomization to the first occurrence of Unstable Angina with Urgent Coronary Revascularization.


Estimated Enrollment: 7500
Study Start Date: May 2010
Estimated Study Completion Date: June 2016
Estimated Primary Completion Date: June 2016 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Febuxostat 40 mg or 80 mg QD
(dependent on serum uric acid levels)
 Drug: Febuxostat
Febuxostat 40 mg or 80 mg (depending on serum uric acid levels), capsules, orally, once daily for up to 60 months.
Other Names:
  • Uloric
  • TMX-67
Active Comparator: Allopurinol 200 mg to 600 mg QD
(dependent on renal function)
 Drug: Allopurinol
Allopurinol 200 mg to 600 mg (depending on renal function), capsules, orally, once daily for up to 60 months.
Other Names:
  • Zyloprim
  • Allohexal
  • Allosig
  • Milurit
  • Alloril
  • Progout
  • Zyloric
  • Puricos
  • Zyrik 300
  • Aluron

Detailed Description:

Gout is caused by high levels of uric acid in the body, and is associated with a broad range of conditions including heart disease, chronic kidney disease and additional risk factors like obesity and high blood pressure. Hyperuricemia, which is defined as an elevation in serum urate levels, develops into gout when urate crystals form from supersaturated body fluids and settle in joints and other organs.

People with gout may also have a higher incidence of other conditions that may be associated with hyperuricemia, gout or both. This is supported by a growing body of research demonstrating that serum urate levels are an independent predictive factor for cardiovascular disease when the effects of other risk factors have been controlled.

This study will explore the cardiovascular safety of febuxostat to determine whether the use of febuxostat is associated with a moderate increase in the risk of serious adverse cardiovascular outcomes as compared to allopurinol.

Participation will last a maximum of 5 years and will include 15 to 20 visits to the study center.

  Eligibility

Ages Eligible for Study:   50 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Has a history of major cardiovascular or cerebrovascular disease including at least one of the following:

    • Myocardial infarction
    • Hospitalized unstable angina
    • Cardiac or cerebrovascular revascularization procedure
    • Stroke
    • Hospitalized for transient ischemic attack
    • Peripheral vascular disease
    • History of diabetes mellitus with evidence of micro- or macrovascular disease

  • Has a history or presence of gout defined as having one or more of the American Rheumatism Association criteria for the diagnosis of gout:

    • A tophus proven to contain urate crystals by chemical or polarized light microscopic means, and/or
    • Characteristic urate crystals in the joint fluid, and/or

    • History of at least 6 of the following clinical, laboratory, and x-ray phenomena:

      • More than 1 attack of acute arthritis
      • Maximum inflammation developed within 1 day
      • Monoarticular arthritis
      • Redness observed over joints
      • First metatarsophalangeal joint painful or swollen
      • Unilateral first metatarsophalangeal joint attack
      • Unilateral tarsal joint attack
      • Tophus (proven or suspected)
      • Hyperuricemia
      • Asymmetric swelling within a joint on x-ray
      • Subcortical cysts without erosions on x-ray
      • Joint fluid culture negative for organisms during attack

  • Must have either:

    • a serum urate level greater than or equal to 7.0 mg/dL at the Day -7 Visit OR
    • a serum urate level greater than or equal to 6.0 mg/dL at the Day -7 Visit AND inadequately controlled gout

Exclusion Criteria:

  • Has secondary hyperuricemia
  • Has a history of xanthinuria
  • Has received urate-lowering or excluded medication during the screening period
  • Has a known hypersensitivity to febuxostat or allopurinol or any components of their formulation
  • Has active peptic ulcer disease
  • Has a history of cancer within 5 years prior to the first dose of study medication
  • Had a myocardial infarction or stroke within 60 days prior to the Screening Visit
  • Has alanine aminotransferase and/or aspartate aminotransferase values greater than 2 times the upper limit of normal during the Screening period
  • Has a history of drug abuse or a history of alcohol abuse within 5 years prior to the Screening Visit or the subject consumes more than14 alcoholic beverages per week
  • Has received any investigational medicinal product within the 30 days prior to the Screening Visit and throughout the study
  • Has an estimated creatinine clearance less than 30 mL/min
  • Is required to take excluded medications
  • Has a known history of infection with hepatitis B, hepatitis C, or human immunodeficiency virus
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01101035

Contacts
Contact: Takeda Study Registration Call Center 888-361-3630 ctgovinfo@goutstudynow.com

  Show 316 Study Locations
Sponsors and Collaborators
Takeda Global Research & Development Center, Inc.
Investigators
Study Director: Senior Medical Director Takeda Global Research & Development Center, Inc.
  More Information

Additional Information:
Uloric Package Insert  This link exits the ClinicalTrials.gov site
FDA Safety Alerts and Recalls  This link exits the ClinicalTrials.gov site
Additional Study Information  This link exits the ClinicalTrials.gov site

No publications provided by Takeda Global Research & Development Center, Inc.

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Responsible Party: Takeda Global Research & Development Center, Inc.
ClinicalTrials.gov Identifier: NCT01101035     History of Changes
Other Study ID Numbers: TMX-67_301, U1111-1114-4194
Study First Received: April 7, 2010
Last Updated: January 17, 2013
Health Authority: United States: Food and Drug Administration

Keywords provided by Takeda Global Research & Development Center, Inc.:
cardiovascular outcomes
heart attack
stroke
Drug Therapy
 physiology
Hyperuricemia
Uric Acid

Additional relevant MeSH terms:
Cardiovascular Diseases
Allopurinol
Febuxostat
Uric Acid
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Pharmacologic Actions
Gout Suppressants
 Antirheumatic Agents
Therapeutic Uses
Free Radical Scavengers
Antioxidants
Antimetabolites
Protective Agents
Physiological Effects of Drugs

ClinicalTrials.gov processed this record on May 23, 2013