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Efficacy and Safety of Abatacept Combined With JAK Inhibitor for Refractory Rheumatoid Arthritis

Z

Zhejiang Provincial People's Hospital

Status and phase

Enrolling
Phase 3

Conditions

Abatacept
Treatment Compliance
Rheumatoid Arthritis

Treatments

Drug: Abatacept
Drug: Janus Kinase Inhibitor

Study type

Interventional

Funder types

Other

Identifiers

NCT05451615
KY2022018

Details and patient eligibility

About

The aim of this study is to observe the clinical efficacy and safety of abatacept combined with JAK inhibitor in the treatment of D2TRA patients

Enrollment

90 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Meet the above diagnostic criteria for refractory rheumatoid arthritis
  2. 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 abatacept combined with a JAK inhibitor is required treated patients

Exclusion criteria

  1. Patients with tumors, hematological diseases, and other autoimmune diseases
  2. Those who have a history of allergies to the drugs selected in this study
  3. Those who cannot adhere to abatacept combined with JAK inhibitor therapy, or who have serious adverse reactions and did not complete the observation period prescribed by the study

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

90 participants in 2 patient groups

Abatacept
Experimental group
Description:
D2T RA patients receive Abatacept
Treatment:
Drug: Abatacept
JAK inhibitor
Experimental group
Description:
D2T RA patients receive JAKi
Treatment:
Drug: Janus Kinase Inhibitor
Drug: Abatacept

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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