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NCT06979271Recruiting

Efficacy and Safety of Telitacicept Combined With Tofacitinib for Refractory Rheumatoid Arthritis

Clinical Efficacy and Safety of Real-world Patients With Refractory Rheumatoid Arthritis (D2TRA) Receiving Telitacicept in Combination With Tofacitinib

Source: ClinicalTrials.gov · Last updated 18 May 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The aim of this study is to observe the clinical efficacy and safety of telitacicept combined with tofacitinib in the treatment of D2TRA patients

Status (registry)
Recruiting
Study type
Observational
Enrollment
20 (estimated)
First submitted
6 May 2025
Start date
Jun 2025
Primary completion date
Apr 2026
Lead sponsor
Zhejiang Provincial People's Hospital
NCT number
NCT06979271

What you commit to

  • Study type: Observational
  • Planned participants: 20
  • From Jun 2025 to the primary completion date, Apr 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Exclusion of patients with severe diseases of major organs (e.g., heart, liver, or lungs)
  • Patients with malignancies, hematological disorders, or other autoimmune diseases (excluding rheumatoid arthritis)
  • History of allergy/hypersensitivity to the study medications (Telitacicept or Tofacitinib)
  • Active tuberculosis or active infectious diseases requiring systemic treatment
  • Failure to complete the prescribed Telitacicept + Tofacitinib regimen due to: Non-adherence or Severe adverse reactions
  • Other conditions contraindicating participation per investigator judgment -

Other

  • Pregnancy, lactation, or refusal to use contraception during the study

Who the study is looking for

  • Age 18-85 years
  • Diagnosed with refractory rheumatoid arthritis according to the 2021 EULAR (European Alliance of Associations for Rheumatology) diagnostic criteria
  • The traditional disease-improving rheumatic drug treatment is ineffective, and the use of two or more biological/targeted disease-improving anti-rheumatic drugs is ineffective, and telitacicept combined with tofacitinib is required treated patients
  • Voluntarily provided written informed consent -

Age in the registry: 18 years to 85 years · Sex: All

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Zhejiang Provincial People's Hospital
Coordinator of this site? Confirm its status
HangzhouChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.