Efficacy of the clinical use of iguratimod therapy in patients with rheumatoid arthritis

Mod Rheumatol. 2015 Mar;25(2):235-40. doi: 10.3109/14397595.2014.938401. Epub 2014 Jul 28.

Abstract

Objective: Iguratimod (IGU) is a new synthetic disease-modifying antirheumatic drug intended to treat patients with rheumatoid arthritis (RA). We conducted a 24-week study on the efficacy of IGU in RA patients with daily clinical use.

Methods: Forty-one patients were enrolled in this study, and the improvement in RA was evaluated every 4 weeks during the 24 weeks.

Results: The patient's global assessment of the disease activity with a scale (Pt VAS) was significantly decreased beginning at week 4. The disease activity score (DAS) 28-erythrocyte sedimentation rate, DAS28-C-reactive protein (CRP), simplified disease activity index and clinical disease activity index all significantly decreased at week 24. The matrix metalloproteinase-3 level was significantly decreased by the combination treatment with methotrexate at week 24. According to a logistic regression analysis, the factor which was most associated with the achievement of low disease activity (DAS28-CRP < 2.7) at week 24 was the DAS28-CRP at week 0.

Conclusions: IGU had significant clinical effects on the RA patients within 24 weeks. IGU might therefore represent a new practical choice to treat RA patients.

Keywords: Cytokine; Disease modifying antirheumatic drugs; Iguratimod; Rheumatoid arthritis; T-614.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antirheumatic Agents / therapeutic use*
  • Arthritis, Rheumatoid / blood
  • Arthritis, Rheumatoid / diagnosis
  • Arthritis, Rheumatoid / drug therapy*
  • Chromones / therapeutic use*
  • Drug Therapy, Combination
  • Female
  • Humans
  • Male
  • Matrix Metalloproteinase 3 / blood
  • Methotrexate / therapeutic use*
  • Middle Aged
  • Severity of Illness Index
  • Sulfonamides / therapeutic use*
  • Treatment Outcome

Substances

  • Antirheumatic Agents
  • Chromones
  • Sulfonamides
  • iguratimod
  • Matrix Metalloproteinase 3
  • Methotrexate