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study on the maintenance strategy of biological agents for elderly rheumatoid arthritis based on treat to target

study on the maintenance strategy of biological agents for elderly rheumatoid arthritis based on treat to target

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075871
Enrollment
Unknown
Registered
2023-09-18
Start date
2023-09-25
Completion date
Unknown
Last updated
2023-09-26

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

Conditions

rheumatoid arthritis

Interventions

clinical remission:Follow up every 12 weeks to evaluate the Treatment to Target. If not reach the target,first increase the TNFi dose to the standard dose, and then adjust the csDMARDs (including meth
If reach the target ,the TNFi was reduced and maintained until the maintenance dose was achieved. The order of reduction was YSP/ETA 50mg QW, 25mg QW, 25mg Q2W (maintenance dose), ADA 40mg Q2W, Q3W, Q
low disease activity group:Follow up every 12 weeks to evaluate the Treatment to Target. If not reach the target,first increase the TNFi dose to the standard dose, and then adjust the csDMARDs (includ

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 85 Years

Inclusion criteria

Inclusion criteria: ?Age = 60 years old; ?Meets the 2010 ACR/Eular classification diagnostic criteria for RA; ?After at least one type of csDMARDs combined with TNFi treatment for = 12 weeks, and the improvement in SDAI= 50% .

Exclusion criteria

Exclusion criteria: Individuals who have participated in clinical trials within the past 6 months. Application of oral corticosteroids during the screening period,or have used glucocorticoids for intra-articular or intramuscular or intravenous injections within the past month. Individuals with a history of active gastric ulcers. Individuals with obvious blood system diseases and abnormal laboratory tests(WBC<4×10^9 /L or PLT<100×10^9/L). ALT?2×ULN,AST?2×ULN,GFR?40ml/min. Individuals with a history of acute or chronic infection (including but not limited to viral hepatitis, herpes zoster virus, tuberculosis, etc.). Individuals with a history of malignant tumors, compensatory dysfunction of heart function, or severe hypertension, epilepsy, and other neurological disorders. Individuals with a history of alcoholism within 2 years.

Design outcomes

Primary

MeasureTime frame
Disease activity index;Adverse reactions;medical expense;

Countries

China

Contacts

Public ContactChen Yingjuan

Beijing Hospital

cyjnew@aliyun.com+86 136 5132 4699

Outcome results

None listed

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