This study will assess the effect of AR882 and XOI co-administration on sUA lowering as well as reducing tophus burden in the population that has failed uricase treatment (eg., pegloticase). Failed uricase treatment is defined as having an inherent intolerance, anaphylaxis, infusion reaction, antibody development, and/or at least one sUA level that rose to greater than 6 mg/dL while on therapy.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
25
Solid Oral Capsule
Solid Oral Tablet
Solid Oral Tablet
Arthrosi Investigative Site (105)
Margate, Florida, United States
RECRUITINGArthrosi Investigative Site (102)
Miami, Florida, United States
RECRUITINGArthrosi Investigative Site (103)
Duncansville, Pennsylvania, United States
RECRUITINGArthrosi Investigative Site (104)
West Lake Hills, Texas, United States
RECRUITINGSerum urate (uric acid) (sUA) level < 6 mg/dL at month 6
Proportion of patients with serum urate (uric acid) (sUA) level \< 6 mg/dL at month 6
Time frame: 24 weeks
Change in tophus burden by month 6
Change in tophus burden by measurement of targeted tophi area at Month 6
Time frame: 24 weeks
Incidence of Adverse Events
Treatment Emergent Adverse Events and Serious Adverse Event incidence
Time frame: 56 weeks
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