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A Prospective Randomized Controlled Trial of IL-1 Monoclonal Antibody for Reducing Arthritis Flare-ups in Gout Patients with Concomitant Chronic Kidney Disease

A Prospective Randomized Controlled Trial of IL-1 Monoclonal Antibody for Reducing Arthritis Flare-ups in Gout Patients with Concomitant Chronic Kidney Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125004
Enrollment
Unknown
Registered
2026-05-20
Start date
2026-05-20
Completion date
Unknown
Last updated
2026-05-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gouty arthritis

Interventions

Anti-IL-1ß monoclonal antibody group:Voxinqibizumab 200mg was administered subcutaneously
Compound Betamethasone group:Compound betamethasone 7mg was given intramuscularly

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with diagnosed gout: meeting the 2015 ACR/EULAR classification criteria for gout 2. Age 18-80 years old 3. At least 2 acute gout attacks in the past 12 months 4. CKD stage 3-4-5 (eGFR = 50mm 6. Inadequate/irresistible response to non-steroidal anti-inflammatory drugs (NSAIDs) and/or colchicine: including: allergy, gastrointestinal reactions (such as nausea, diarrhea, dyspepsia, etc.), elevated liver and kidney function, agranulocytosis, thrombocytopenia; poor efficacy of joint pain treatment, etc. 7. Signed informed consent form, agreeing to participate in this study

Exclusion criteria

Exclusion criteria: 1.Active complications: Active infection, active gastrointestinal bleeding, or severe immunosuppression. 2.Recent cardiovascular events: Serious cardio-cerebrovascular events within the last 6 months. 3.Hypersensitivity: Known allergy to any components of the study medications. 4.Pregnancy/Lactation: Women who are pregnant, breastfeeding, or planning to become pregnant. 5.General Ineligibility: Poor compliance, psychiatric disorders, or any other conditions that, in the investigator’s judgment, make the patient unsuitable for the study.

Design outcomes

Primary

MeasureTime frame
Time to First Gout Flare;

Secondary

MeasureTime frame
Safety;Renal function;Living Care score;

Countries

China

Contacts

Public ContactYu Wang

Peking University First Hospital

wangyu@163.com+86 136 9337 4001

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 30, 2026