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Recruiting Phase 1 NCT06298071

A Phase Ib Clinical Trial of Peguricase for Injection With Methotrexate in Patients With Uncontrolled Gout.

Trial Parameters

Condition Gout
Sponsor Shanghai Institute Of Biological Products
Study Type INTERVENTIONAL
Phase Phase 1
Enrollment 36
Sex ALL
Min Age 18 Years
Max Age 70 Years
Start Date 2023-03-03
Completion 2026-12-30
Interventions
SIBP-R002SIBP-R002SIBP-R002

Brief Summary

To evaluate the safety and tolerability of peguricase for injection with methotrexate in patients with gout who remain uncontrolled after standardized treatment with conventional uric acid-lowering drugs, to determine the recommended dose for phase II clinical trials, and to provide basis for formulation of administration regimen for phase II clinical trials.

Eligibility Criteria

Inclusion Criteria: * Willing and able to give informed consent. * Male and female aged between 18 and 70 years old , regardless of gender. * Male weight ≥50 kg, female weight ≥45 kg, body mass index (BMI) in the range of (19-30) kg/m2 (including 19 and 30); * The clinical diagnosis of gout met the criteria of American College of Rheumatology (ACR)/European League Against Rheumatism (EULAR) in 2015,patients were in non-acute attack at screening or at least 2 weeks after complete remission of acute attack, and sUA ≥420 μmol/L at screening; * Patients whose serum uric acid level could not reach the target after standard treatment with conventional uric acid-lowering drugs or who were contraindicated or intolerant to conventional uric acid-lowering drugs; * Patients who were willing to stop taking any uric-acid-lowering drug at least 7 days before using methotrexate during the run-in period; * Could tolerate the prescribed dose of methotrexate during the run-in period; * Patients were abl

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