The Journal of the Korean Rheumatism Association 2005; 12(4): 291-303
Published online December 30, 2005
© Korean College of Rheumatology
성윤경·고은미*·박원**·이수곤***·이지수†·김철준‡·박영주‡·배상철
한양대학교 의과대학 내과학교실 류마티스병원, 성균관대학교 의과대학 삼성서울병원 내과학교실*, 인하대학교 의과대학 내과학교실**, 연세대학교 의과대학 내과학교실***, 이화여자대학교 의과대학 내과학교실†, 한국엠에스디(주)‡
Correspondence to : Sang-Cheol Bae
Objective: To assess the efficacy and the safety of etoricoxib 90 mg daily administered to Korean patients for the treatment of rheumatoid arthritis over a 12-week period. Methods: Eighty-nine patients diagnosed with rheumatoid arthritis were administered Etoricoxib 90 mg for 12 weeks. Tender Joint Count (total 68 joints), Swollen Joint Count (total 66 joints), Patient Global Assessment of Disease Activity, and Investigator Global Assessment of Disease Activity were assessed as primary endpoints. Patient Global Assessment of Pain, Health Assessment of Questionnaire (HAQ: disability scales), Patient Global Assessment of Response to Therapy, Investigator Global Assessment of Response to Therapy, and Duration of Morning Stiffness were assessed as secondary endpoints. Those endpoints were assessed at week 2, 4, 8, and 12. Safety was evaluated by physical examination, serum chemistry, blood count, urinalysis, and occurrence of adverse events.Results: Etoricoxib 90 mg showed significant effects compared to baseline, thus the result indicated etoricoxib was clinically effective. Etoricoxib 90 mg showed significant improvement in all efficacy endpoints (primary endpoints and secondary endpoints). Treatment effects for etoricoxib 90 mg were approximately a 7.3 (95% CI 5.8 8.9, p<0.0001) joint reduction in the number of tender joints, 4.8 (95% CI 3.6 6.0, p<0.0001) joint reduction in the number of swollen joints, a 15.4 (95% CI 12.1 18.7, p<0.0001) mm improvement in the patient global assessment (100 mm VAS) and 1.3 (95% CI 1.1 1.6, p<0.0001) unit improvement in the investigator global assessment (0 to 4 Likert scale). Treatment effects were observed at the earliest time point of measurement and were maintained over time during the 12-week period. Drug-related clinical adverse events were reported by 22 (24.7%) of 89 safety evaluable subjects. Eight patients discontinued the drug due to clinical adverse events. Frequency of drug-related laboratory abnormalities was low with 2 (2.2%). Nobody discontinued due to laboratory abnormalities. Conclusion: (1) Etoricoxib 90 mg once daily was clinically effective for the treatment of rheumatoid arthritis in Korea patients. (2) Etoricoxib 90 mg once daily administered to patients with rheumatoid arthritis was generally safe and well tolerated.
Keywords Rheumatoid arthritis, Etoricoxib, Efficacy, Adverse experience
The Journal of the Korean Rheumatism Association 2005; 12(4): 291-303
Published online December 30, 2005
Copyright © Korean College of Rheumatology.
성윤경·고은미*·박원**·이수곤***·이지수†·김철준‡·박영주‡·배상철
한양대학교 의과대학 내과학교실 류마티스병원, 성균관대학교 의과대학 삼성서울병원 내과학교실*, 인하대학교 의과대학 내과학교실**, 연세대학교 의과대학 내과학교실***, 이화여자대학교 의과대학 내과학교실†, 한국엠에스디(주)‡
Yoon-Kyoung Sung, M.D., Eun-Mi Koh, M.D.*, Won Park, M.D.**, Soo-Kon Lee, M.D.***, Jisoo Lee, M.D.†, Chul Joon Kim, M.D.‡, Young Joo Park, M.D.‡, Sang-Cheol Bae, M.D.*
Department of Internal Medicine, the Hospital for Rheumatic Diseases, Hanyang University College of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine*, Seoul, College of Medicine, Inha University**, Incheon, Yonsei Universisy College of Medicine***, Ewha Womans University College of Medicine†, Seoul, MSD Korea‡, Gwangju, Korea
Correspondence to:Sang-Cheol Bae
Objective: To assess the efficacy and the safety of etoricoxib 90 mg daily administered to Korean patients for the treatment of rheumatoid arthritis over a 12-week period. Methods: Eighty-nine patients diagnosed with rheumatoid arthritis were administered Etoricoxib 90 mg for 12 weeks. Tender Joint Count (total 68 joints), Swollen Joint Count (total 66 joints), Patient Global Assessment of Disease Activity, and Investigator Global Assessment of Disease Activity were assessed as primary endpoints. Patient Global Assessment of Pain, Health Assessment of Questionnaire (HAQ: disability scales), Patient Global Assessment of Response to Therapy, Investigator Global Assessment of Response to Therapy, and Duration of Morning Stiffness were assessed as secondary endpoints. Those endpoints were assessed at week 2, 4, 8, and 12. Safety was evaluated by physical examination, serum chemistry, blood count, urinalysis, and occurrence of adverse events.Results: Etoricoxib 90 mg showed significant effects compared to baseline, thus the result indicated etoricoxib was clinically effective. Etoricoxib 90 mg showed significant improvement in all efficacy endpoints (primary endpoints and secondary endpoints). Treatment effects for etoricoxib 90 mg were approximately a 7.3 (95% CI 5.8 8.9, p<0.0001) joint reduction in the number of tender joints, 4.8 (95% CI 3.6 6.0, p<0.0001) joint reduction in the number of swollen joints, a 15.4 (95% CI 12.1 18.7, p<0.0001) mm improvement in the patient global assessment (100 mm VAS) and 1.3 (95% CI 1.1 1.6, p<0.0001) unit improvement in the investigator global assessment (0 to 4 Likert scale). Treatment effects were observed at the earliest time point of measurement and were maintained over time during the 12-week period. Drug-related clinical adverse events were reported by 22 (24.7%) of 89 safety evaluable subjects. Eight patients discontinued the drug due to clinical adverse events. Frequency of drug-related laboratory abnormalities was low with 2 (2.2%). Nobody discontinued due to laboratory abnormalities. Conclusion: (1) Etoricoxib 90 mg once daily was clinically effective for the treatment of rheumatoid arthritis in Korea patients. (2) Etoricoxib 90 mg once daily administered to patients with rheumatoid arthritis was generally safe and well tolerated.
Keywords: Rheumatoid arthritis, Etoricoxib, Efficacy, Adverse experience
Roshan Subedi, M.D., Afrah Misbah, M.D., Adnan Al Najada, M.D., Anthony James Ocon, M.D., Ph.D.
J Rheum Dis -0001; ():Hee Jun Kim, R.N., Ph.D., Ju-Yang Jung, M.D., Ph.D., Ji-Won Kim, M.D., Chang-Hee Suh, M.D., Ph.D., Hyoun-Ah Kim, M.D., Ph.D.
J Rheum Dis -0001; ():In-Woon Baek, M.D., Kyung-Su Park, M.D., Ph.D., Ki-Jo Kim, M.D., Ph.D.
J Rheum Dis -0001; ():