Clinical trial

CSP #594 - Comparative Effectiveness in Gout: Allopurinol vs. Febuxostat

Name
594
Description
This trial will compare two effective therapies, allopurinol and febuxostat, to lower serum uric acid and therefore prevent further gout attacks. These therapies have never been compared at appropriate doses. Further, they will be studied in patients with kidney disease for the first time.
Trial arms
Trial start
2017-03-06
Estimated PCD
2021-02-01
Trial end
2021-04-15
Status
Completed
Phase
Early phase I
Treatment
allopurinol capsule, 100-800 mg by mouth once daily
Patients will be up-titrated up to the dose required to reach target uric acid levels.
Arms:
Allopurinol / Sham Comparator (Febuxostat)
Other names:
Zyloprim; CAS: 315-30-0
febuxostat tablet 40-120 mg by mouth once daily
Patients will be up-titrated to the dose required to reach target uric acid levels.
Arms:
Febuxostat / Sham Comparator (Allopurinol)
Other names:
Uloric; CAS: 144060-53-7; NDCs: 64764-677-11, 64764-677-13, 64764-677-19, 64764-677-30, 64764-918-11, 64764-918-18, 64764-918-30, 64764-918-90
Placebo, vehicle control (febuxostat-shaped)
Placebo tablets resembling febuxostat will be given with allopurinol.
Arms:
Allopurinol / Sham Comparator (Febuxostat)
Placebo, vehicle control (allopurinol-shaped)
Placebo capsules resembling allopurinol will be given with febuxostat.
Arms:
Febuxostat / Sham Comparator (Allopurinol)
Size
950
Primary endpoint
Percentage of Participants Experiencing ≥ 1 Gout Flare During Phase 3
Phase III of the study (weeks 49-72 of study duration)
Eligibility criteria
Inclusion Criteria: * Age 18 years * History of gout - crystal proven or historical as defined by ACR criteria listed above * Serum urate level \> 6.8 mg/dl Exclusion Criteria: * Stage 4 or 5 Chronic Kidney Disease (CKD) - defined as eGFR \< 30 ml/min/1.73 m2 * Women less than 50 years of age * Patients with a history of prior solid organ / hematopoietic transplantation * Previous allergy or intolerance to allopurinol or febuxostat * Patients who are not candidates for any of the recommended prophylactic medications (colchicine, naprosyn or glucocorticoids) * Patients who in the opinion of the investigator have a high genetic risk for allopurinol hypersensitivity syndrome (AHS\*) unless they have been found to be negative for HLA B5801. * Previous history of failure to reach target uric acid levels despite therapy with allopurinol at dose \> 300 mg/day * Prior febuxostat use * Patients with malignancies that are currently active with exception of non-melanoma skin cancer * Patients with serum uric acid levels \>15 mg/dl * Patients with myelodysplasia and hemoglobin of \< 8.5 mg/dL * Patients with chronic liver disease with more than one of the following: * INR \> 1.7, not on Warfarin therapy * Bilirubin 2 mg/dL * Serum albumin \< 3.5 mg/dL * Ascites * Encephalopathy * Current use of azathioprine, mercaptopurine, didanosine, cyclophosphamide, probenecid, lesinurad or pegloticase * Enrollment in another randomized interventional clinical trial * Any severe medical condition that, in the enrolleer's opinion, is likely to compromise the participant's ability to complete the trial
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE4'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 950, 'type': 'ACTUAL'}}
Updated at
2024-03-29

1 organization

3 products

2 indications

Indication
Gout
Product
Febuxostat
Product
Placebo