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The effect and safety of Tocilizumab on treating Takayasu's arteritis

The effect and safety of Tocilizumab on treating Takayasu's arteritis

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPC-16009231
Enrollment
Unknown
Registered
2016-09-20
Start date
2016-10-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Takayasu's arteritis

Interventions

Tocilizumab treatment group:Tocilizumab treatment group

Sponsors

Department of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Males or non-pregnant female aged older than 18 years, fulfilled the TA classification criteria of the American College of Rheumatology (ACR), diagnosed with active disease state according to the National Institute of Health (NIH) criteria, whether they were treated by na?ve or not, and those who had never received TCZ before.

Exclusion criteria

Exclusion criteria: 1) un-controlled diabetes, hypertension before entry; 2) active digestive tract bleeding 3 months before entry; 3) history of or active primary or secondary immunodeficiency, and malignant diseases; 4) active infections that requires treatment or not, including bacteria, virus, fungi and mycobacteria infection; 5) neutrophil counts < 1.0×10^9/L, platelet counts < 100×10^9/L; 6) alanine aminotransferase (ALT) or aspartate aminotransferase (AST) level?2 times the upper normal limit (UNL), serum creatinine level?1.5 UNL.^

Design outcomes

Primary

MeasureTime frame
Erythrocyte sedimentation rate level before and after Tocilizumab treatment;hyper-sensitive C reactive protein before and after Tocilizumab treatment;Mural thickness of common carotid artery before and after Tocilizumab treatment;Mural thickness of subclavian artery before and after Tocilizumab treatment;Glucocoticoid dosage before and after Tocilizumab treatment;The adverse events of Tocilizumab;

Countries

China

Contacts

Public ContactXinping TIAN

Department of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital

tianxp6@126.com+86 13691165939

Outcome results

None listed

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