This is a multicenter, randomized, double-blind, placebo-controlled phase II study assessing the efficacy, safety, and dosing regimen selection of multiple IV infusions of PRX-115 over 24 weeks, with or without MTX, versus the respective placebos in adult patients with gout.
This study will evaluate the efficacy, safety, tolerability, immunogenicity, pharmacokinetics (PK), and pharmacodynamics (PD) of PRX-115 (a recombinant pegylated Uricase) in adult patients with gout. Participants will receive PRX-115 by intravenous (IV) infusions according to different treatment schedules, with and without the immunomodulator methotrexate (MTX).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
150
intravenous (IV) infusion
Oral MTX 15 mg weekly
intravenous (IV) infusion
Bioclinical Research Alliance, Inc
Miami, Florida, United States
RECRUITINGPercentage of Serum Uric Acid (sUA) Responders (sUA < 6 mg/dL) During Month 6
Proportion of patients who achieve a reduction in sUA to \<6.0 mg/dL for at least 80% of the time during Month 6
Time frame: 6 months of treatment
Percentage of Serum Uric Acid (sUA) Responders (sUA < 6 mg/dL) at different time points
Proportion of patients that achieve a reduction in sUA to \<6.0 mg/dL for at least 80% of the time during Month 3 or 4, 5 and 6.
Time frame: 3 to 6 months of treatment
Treatment-emergent adverse events (TEAEs)
Occurrence and severity of treatment-emergent adverse events (TEAEs)
Time frame: From enrollment to 8 months of study
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Oral Placebo-MTX weekly