Efficacy and Safety of Telitacicept Combined With Baricitinib for Refractory Rheumatoid Arthritis (NCT07491016) | Clinical Trial Compass
RecruitingNot Applicable
Efficacy and Safety of Telitacicept Combined With Baricitinib for Refractory Rheumatoid Arthritis
China30 participantsStarted 2026-03-01
Plain-language summary
The aim of this study is to observe the clinical efficacy and safety of telitacicept combined with baricitinib in the treatment of D2TRA patients
Who can participate
Age range18 Years – 85 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* 1\. Age 18-85 years
* 2\. Diagnosed with refractory rheumatoid arthritis according to the 2021 EULAR (European Alliance of Associations for Rheumatology) diagnostic criteria
* 3\. 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
* 4\. Voluntarily provided written informed consent
Exclusion Criteria:
* 1\. Exclusion of patients with severe diseases of major organs (e.g., heart, liver, or lungs)
* 2\. Patients with malignancies, hematological disorders, or other autoimmune diseases (excluding rheumatoid arthritis)
* 3\. History of allergy/hypersensitivity to the study medications (Telitacicept or Tofacitinib)
* 4\. Active tuberculosis or active infectious diseases requiring systemic treatment
* 5\. Pregnancy, lactation, or refusal to use contraception during the study
* 6\. Failure to complete the prescribed Telitacicept + Tofacitinib regimen due
* to:Non-adherence or Severe adverse reactions
* 7\. Other conditions contraindicating participation per investigator judgment
What they're measuring
1
Efficacy of Telitacicept Combined With Baricitinib for Refractory Rheumatoid Arthritis