Efficacy and safety of febuxostat extended release and immediate release in patients with gout and moderate renal impairment: Phase II placebo-controlled study

Academic Article


  • © 2018 The Author(s). Background: Febuxostat immediate release (IR), a xanthine oxidase inhibitor, is indicated for the management of hyperuricemia in patients with gout by lowering urate levels. An extended release (XR) formulation of febuxostat was developed to provide equal or superior efficacy on urate lowering compared with the IR formulation and potentially lower the risk of treatment-initiated gout flares due to an altered pattern of drug exposure. The present study evaluated the efficacy and safety of febuxostat XR and IR formulations in patients with gout and moderate renal impairment (estimated glomerular filtrate rate≥30 and<60ml/min). Methods: This was an exploratory, 3-month, phase II, multicenter, placebo-controlled, double-blind proof-of-concept study. Patients (n=189) were randomized 1:1:1:1:1 to receive placebo or febuxostat IR 40mg, XR 40mg, IR 80mg, or XR 80mg once daily. Endpoints included: proportion of patients with serum uric acid (sUA) <5.0mg/dl at month 3 (primary endpoint), proportion of patients with sUA <6.0mg/dl at month 3, and proportion of patients with ≥1 gout flare requiring treatment over 3months. Results: At month 3, all febuxostat treatment groups were associated with greater proportions of patients achieving sUA <5.0mg/dl (p<0.05 vs placebo). A greater proportion of patients receiving XR 40mg achieved sUA <5.0mg/dl versus those receiving IR 40mg (p=0.034); proportions were similar in the IR 80mg and XR 80mg groups. Higher proportions of febuxostat-treated patients achieved sUA <6.0mg/dl at month 3 (p<0.05 vs placebo) and experienced ≥1 gout flare (significant for all comparisons, except XR 40mg). Incidences of treatment-related adverse events were low across all treatment groups; the majority were mild or moderate with no apparent trends correlating with IR or XR doses. The most common treatment-emergent adverse event was hypertension. One death (unrelated to the study drug) was reported. Conclusions: These exploratory data demonstrate that febuxostat (XR and IR) formulations were effective and well tolerated in patients with gout and moderate renal impairment.
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  • Gunawardhana L; Becker MA; Whelton A; Hunt B; Castillo M; Saag K
  • Volume

  • 20
  • Issue

  • 1