Overview

This trial is active, not recruiting.

Condition cardiovascular disease
Treatments febuxostat, allopurinol
Phase phase 3
Sponsor Takeda
Collaborator Teijin America, Inc.
Start date April 2010
End date December 2018
Trial size 6198 participants
Trial identifier NCT01101035, TMX-67_301, U1111-1114-4194

Summary

The purpose of this study is to see whether subjects with gout who receive febuxostat or allopurinol for up to 9 years have a higher rate of serious heart and blood vessel complications (major cardiovascular events). Examples of major cardiovascular events include heart attacks, strokes, and angina (chest pain due to narrowing of the blood vessels of the heart) that need to be treated urgently with a heart operation. The overall duration of the study is dependent on the number of predefined major cardiovascular events (MACE). The length of study is expected to be approximately 9 years in order to observe the required 624 MACE. The length of study participation for each subject will vary due to the event driven study design.

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.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification safety study
Intervention model parallel assignment
Masking double blind (subject, caregiver, investigator, outcomes assessor)
Primary purpose treatment
Arm
(Experimental)
(dependent on serum uric acid levels)
febuxostat Uloric
Febuxostat 40 mg or 80 mg (depending on serum uric acid levels), capsules, orally, once daily for up to 60 months.
(Active Comparator)
(dependent on renal function)
allopurinol Zyloprim
Allopurinol 200 mg to 600 mg (depending on renal function), capsules, orally, once daily for up to 60 months.

Primary Outcomes

Measure
First occurrence of any event in the predefined Major Adverse Cardiovascular Events Composite.
time frame: At first occurrence (up to 60 Months)

Secondary Outcomes

Measure
First occurrence of any Antiplatelet Trialists' Collaborative Event.
time frame: At first occurrence (up to 60 Months)
First occurrence of Cardiovascular Death death.
time frame: At first occurrence (up to 60 Months)
First occurrence of Non-fatal Myocardial Infarction.
time frame: At first occurrence (up to 60 Months)
First occurrence of Non-fatal stroke.
time frame: At first occurrence (up to 60 Months)
First occurrence of Unstable Angina with Urgent Coronary Revascularization.
time frame: At first occurrence (up to 60 Months)

Eligibility Criteria

Male or female participants at least 50 years old.

Inclusion Criteria: 1. The subject or the subject's legally acceptable representative signs and dates a written, informed consent form/Health Insurance Portability and Accountability Act (HIPAA) Authorization prior to the initiation of any study procedures. 2. The subject is male ≥50 years of age or female ≥55 years of age and at least 2-years post-menopausal. 3. The subject has a history of major CV or cerebrovascular disease including at least one of the following: - MI. - Hospitalized unstable angina. - Cardiac or cerebrovascular revascularization procedure. - Stroke. - Hospitalized TIA. - Peripheral vascular disease (ankle brachial index ≤0.6, revascularization and/or well-documented history of claudication). - History of diabetes mellitus with evidence of micro- or macrovascular disease (retinopathy, neuropathy, nephropathy, small vessel vascular diseases). 4. The subject 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. 5. The subjects must have either: - a sUA level ≥7.0 mg/dL (≥416 μmol/L) at the Day -7 Visit OR - a sUA level ≥6.0 mg/dL (≥354 μmol/L) at the Day -7 Visit AND inadequately controlled gout (≥1 flare in the 12 months prior to screening and/or the presence of tophi). 6. The subject is capable of understanding and complying with protocol requirements Exclusion Criteria: Subjects who meet any of the following criteria will not qualify for entry into this study: 1. The subject has secondary hyperuricemia (eg, due to myeloproliferative disorder, or organ transplant). 2. The subject has a history of xanthinuria. 3. The subject has received urate-lowering therapy (i.e., febuxostat, allopurinol, probenecid, etc.) or excluded medication during the screening period (beginning with Day -7). 4. The subject has a known hypersensitivity to febuxostat or allopurinol or any components of their formulation. 5. The subject has active peptic ulcer disease. 6. The subject has a history of cancer (other than basal cell carcinoma of the skin) within 5 years prior to the first dose of study medication. 7. The subject had MI or stroke within 60 days prior to the Screening Visit. 8. The subject has ALT and/or AST values greater than 2 times the upper limit of normal (×ULN) during the Screening period. 9. The subject has a significant medical condition and/or conditions that would interfere with the treatment, safety, or compliance with the protocol. 10. The subject has a history of drug abuse (defined as any illicit drug use) or a history of alcohol abuse within 5 years prior to the Screening Visit or the subject consumes >14 alcoholic beverages per week. 11. The subject has received any investigational medicinal product within the 30 days prior to the Screening Visit and throughout the study. 12. The subject's estimated CLcr is <30 mL/min, where CLcr is calculated using the Cockcroft and Gault formula based on ideal body weight (IBW), 13. The subject is an immediate family member, study site employee, or is in a dependant relationship with a study site employee who is involved in conduct of this study (eg, spouse, parent, child, sibling) or may consent under duress. 14. The subject is required to take excluded medications 15. The subject has a known history of infection with hepatitis B, hepatitis C, or human immunodeficiency virus. 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

Additional Information

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
Description This is a phase 3B multicenter, randomized, double-blind, active-controlled study designed to evaluate the cardiovascular (CV) safety of febuxostat compared with allopurinol in subjects with gout and significant CV comorbidities. Approximately 7500 subjects, males 50 years of age or older or females 55 years of age or older (at least 2-years post-menopausal), with gout and health problems affecting the heart or blood vessels will take part in this study at approximately 450 study centers in North America. This study will use competitive enrollment. This means that when a target number of subjects has entered the treatment phase of the study, all further screening of subjects will be closed. The length of the study is based on an ongoing review of study results. The participation will last a maximum of 9 years and will include a maximum 28 visits to the study center. Telephone contact will be made every 2 months for subjects who have discontinued the study drug for any reason, but who are asked to continue in the study to be followed for potential cardiovascular events. This study design is called a "Time to Event Study". All study subjects will continue to be followed until enough information has been gathered to determine the overall safety of the study drug. 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.
Trial information was received from ClinicalTrials.gov and was last updated in August 2016.
Information provided to ClinicalTrials.gov by Takeda.