Skip to content

A real-world study of tocilizumab (LZM008) in the treatment of rheumatoid arthritis (RA)

A real-world study of tocilizumab (LZM008) in the treatment of rheumatoid arthritis (RA)

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500096500
Enrollment
Unknown
Registered
2025-01-24
Start date
2025-01-30
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Rheumatoid arthritis

Interventions

Experimental group:none

Sponsors

Affiliated Hospital of North Sichuan Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patient age>= 18 years old; 2.Diagnosed by a doctor with rheumatoid arthritis, meeting the diagnostic criteria for RA classification formulated by ACR/EULAR in 2010; 3. RA disease activity (DAS28>=2.6); 4. No prior treatment with tocilizumab; 5.Good compliance and follow-up.

Exclusion criteria

Exclusion criteria: 1. Live vaccine immunization within 4 weeks prior to screening; 2.History of underlying tuberculosis infection or tumor; 3.acute or chronic active infection; 4.Accompanied by other diffuse connective tissue diseases such as systemic lupus erythematosus, severe knee osteoarthritis and Sjogren's syndrome; 5. Severe hepatic and renal insufficiency; 6.Severe heart, brain and vascular lesions; 7. Pregnant or lactating women; 8.Treatment with any biologic agent within 4 weeks (or 5 half-lives of the investigational drug, whichever is longer) prior to initiation of tocilizumab therapy 9.Those who have mental disorders, a history of alcoholism, immunodeficiency, drug or other substance abuse; 10.Those who are allergic to the ingredients of this product; 11.Those who are judged by the investigator to be unable to comply with the requirements of the study or who withdraw voluntarily.

Design outcomes

Primary

MeasureTime frame
Proportion of subjects achieving ACR20 at week 24 after the first dose;

Secondary

MeasureTime frame
28 levels of joint disease activity;Clinical Disease Activity Index;

Countries

China

Contacts

Public ContactQing Yufeng

Affiliated Hospital of North Sichuan Medical College

qingyufengqq@163.com+86 158 8265 7267

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026