Rofecoxib, a specific inhibitor of cyclooxygenase 2, with clinical efficacy comparable with that of diclofenac sodium - Results of a one-year, randomized, clinical trial in patients with osteoarthritis of the knee and hip

被引:0
|
作者
Cannon, GW
Caldwell, JR
Holt, P
McLean, B
Seidenberg, B
Bolognese, J
Ehrich, E
Mukhopadhyay, S
Daniels, B
机构
[1] Merck & Co Inc, Rahway, NJ 07065 USA
[2] Univ Utah, Salt Lake City, UT USA
[3] Dept Vet Affairs Med Ctr, Salt Lake City, UT USA
来源
ARTHRITIS AND RHEUMATISM | 2000年 / 43卷 / 05期
关键词
D O I
10.1002/1529-0131(200005)43:5<978::AID-ANR4>3.0.CO;2-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To compare the clinical efficacy of rofecoxib, a specific inhibitor of cyclooxygenase 2 (COX-2), with that of diclofenac in patients with osteoarthritis (OA) and to evaluate the safety and tolerability of rofecoxib. Methods. We performed a randomized, double-blind, active comparator-controlled trial in 784 adults with OA of the knee or hip. Patients were randomized to 1 of 3 treatment groups: 12.5 mg of rofecoxib once daily, 25 mg of rofecoxib once daily, and 50 mg of diclofenac 3 times daily. Clinical efficacy and safety were evaluated over a 1-year continuous treatment period. Results. Rofecoxib at dosages of 12.5 and 25 mg demonstrated efficacy that was clinically comparable to that of diclofenac, as assessed by all 3 primary end points according to predefined comparability criteria. Results from secondary end points were consistent with those of the primary end points. There were small statistical differences favoring diclofenac for 2 of the end points. All treatments were well tolerated. Conclusion. Rofecoxib was well tolerated and provided efficacy that was clinically comparable, according to predefined statistical criteria, to that of 150 mg of diclofenac per day in this 1-year study. Specific inhibition of COX-2 provided therapeutic efficacy in OA.
引用
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页码:978 / 987
页数:10
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