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Clinical Trial Summary

The study will establish efficacy and safety of rasburicase in chronic gouty arthritis


Clinical Trial Description

The study hypothesis is that the proportion of patients who achieved the primary endpoint after 12 weeks of treatment with rasburicase combined with oral urate-lowering therapy is superior to 12 weeks of treatment with oral urate-lowering therapy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05312268
Study type Interventional
Source Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Contact Qianhua Li, M.D.&Ph.D
Phone 862081332572
Email liqianhua@mail.sysu.edu.cn
Status Recruiting
Phase Phase 4
Start date June 15, 2022
Completion date April 15, 2025

See also
  Status Clinical Trial Phase
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Completed NCT02956278 - The Effects of BCRP Q141K on Allopurinol Pharmacokinetics and Dynamics Phase 4
Completed NCT03905512 - A Study to Compare the Efficacy of SEL-212 to KRYSTEXXA® in Gout Participants Refractory to Conventional Therapy Phase 2
Completed NCT04762498 - A Phase 4, Open-label Study of KRYSTEXXA® (Pegloticase) Co-administered With Methotrexate (MTX) in Patients With Uncontrolled Gout (FORWARD OL) Phase 4
Completed NCT04513366 - A Study of SEL-212 in Patients With Gout Refractory to Conventional Therapy Phase 3