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Peer-reviewedCC BY 4.0Journal of Clinical Medicine

The Clinical Factors Related to the Efficacy of Ozoralizumab in Patients with Rheumatoid Arthritis

  1. 1Nippori Orthopaedics and Rheumatic Clinic, Tokyo 116-0014, Japan
  2. 2Toho University Omori Medical Center, Tokyo 143-8541, Japan

Abstract

Background/Objectives: Ozoralizumab, a tumor necrosis factor (TNF) blocker, was launched in Japan in 2022. However, there is no evidence to determine whether this biological agent is the best choice for patients with rheumatoid arthritis (RA). To investigate the clinical factors related to the efficacy of ozoralizumab, we analyzed 100 patients treated with ozoralizumab in real-world practice. Methods: 100 patients with RA treated with ozoralizumab (female, n = 87; male, n = 13), with a mean age of 61.8 years, and a mean disease duration of 10.7 years. Methotrexate (MTX) and prednisolone (PSL) were used by 49% and 10% of patients, respectively. The cohort included biologic-naïve patients (n = 39) and patients who switched from another biologic agent (n = 61). Rheumatoid factor (RF) and anti-cyclic citrullinated peptide (anti-CCP) positivity rates were 91% and 74%, respectively. We analyzed clinical factors associated with Disease Activity Score 28 C-reactive protein (DAS28-CRP) at 24 weeks and assessed remission, treatment continuation, and adverse-event rates. Results: DAS28-CRP decreased from 4.38 at baseline to 2.59 at 24 weeks. The remission rate was 59% at 24 weeks. DAS28-CRP at 24 weeks correlated with the anti-CCP titer in the MTX-positive group. Disease duration was correlated with DAS28-CRP at 24 weeks in the MTX-negative and biologic-naïve groups. Remission at 24 weeks was correlated with disease duration. Adverse events occurred in 9% of patients, and all cases improved. Conclusions: The efficacy and safety of ozoralizumab were confirmed in 100 patients with RA. Anti-CCP and disease duration are clinical factors that may predict the efficacy of ozoralizumab in RA. Therefore, a high anti-CCP titer or early RA may indicate the efficacy of ozoralizumab in real-world RA practice.

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BibTeX
@article{kanbe2026clinical,
  title = {{The Clinical Factors Related to the Efficacy of Ozoralizumab in Patients with Rheumatoid Arthritis}},
  author = {Katsuaki Kanbe and Ayako Kubota},
  journal = {Journal of Clinical Medicine},
  year = {2026},
  month = nov,
  doi = {10.3390/jcm15218603},
  url = {https://www.mdpi.com/2077-0383/15/21/8603},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - The Clinical Factors Related to the Efficacy of Ozoralizumab in Patients with Rheumatoid Arthritis
AU  - Katsuaki Kanbe
AU  - Ayako Kubota
PY  - 2026
DA  - 2026/11/04
JO  - Journal of Clinical Medicine
DO  - 10.3390/jcm15218603
UR  - https://www.mdpi.com/2077-0383/15/21/8603
AB  - Background/Objectives: Ozoralizumab, a tumor necrosis factor (TNF) blocker, was launched in Japan in 2022. However, there is no evidence to determine whether this biological agent is the best choice for patients with rheumatoid arthritis (RA). To investigate the clinical factors related to the efficacy of ozoralizumab, we analyzed 100 patients treated with ozoralizumab in real-world practice. Methods: 100 patients with RA treated with ozoralizumab (female, n = 87; male, n = 13), with a mean age of 61.8 years, and a mean disease duration of 10.7 years. Methotrexate (MTX) and prednisolone (PSL) were used by 49% and 10% of patients, respectively. The cohort included biologic-naïve patients (n = 39) and patients who switched from another biologic agent (n = 61). Rheumatoid factor (RF) and anti-cyclic citrullinated peptide (anti-CCP) positivity rates were 91% and 74%, respectively. We analyzed clinical factors associated with Disease Activity Score 28 C-reactive protein (DAS28-CRP) at 24 weeks and assessed remission, treatment continuation, and adverse-event rates. Results: DAS28-CRP decreased from 4.38 at baseline to 2.59 at 24 weeks. The remission rate was 59% at 24 weeks. DAS28-CRP at 24 weeks correlated with the anti-CCP titer in the MTX-positive group. Disease duration was correlated with DAS28-CRP at 24 weeks in the MTX-negative and biologic-naïve groups. Remission at 24 weeks was correlated with disease duration. Adverse events occurred in 9% of patients, and all cases improved. Conclusions: The efficacy and safety of ozoralizumab were confirmed in 100 patients with RA. Anti-CCP and disease duration are clinical factors that may predict the efficacy of ozoralizumab in RA. Therefore, a high anti-CCP titer or early RA may indicate the efficacy of ozoralizumab in real-world RA practice.
SN  - 2077-0383
ER  -