Rofecoxib, a new cyclooxygenase 2 inhibitor, shows sustained efficacy, comparable with other nonsteroidal anti-inflammatory drugs: a 6-week and a 1-year trial in patients with osteoarthritis. Osteoarthritis Studies Group.

K Saag, D van der Heijde, C Fisher, A Samara, L DeTora, J Bolognese, R Sperling, B Daniels
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引用次数: 119

Abstract

Introduction: Rofecoxib, a cyclooxygenase 2 inhibitor (sometimes known as a specific cyclooxygenase 2 inhibitor or Coxib), is used in osteoarthritis (OA). Published information indicates rofecoxib's improved gastrointestinal safety profile over nonselective nonsteroidal anti-inflammatory agents (NSAIDs).

Objective: To evaluate the efficacy and safety of rofecoxib in treating OA in 2 studies.

Methods: Two randomized, double-blind, parallel-group studies in patients with OA of the knee or hip were conducted using identical entry criteria and end points. A 6-week placebo-controlled trial in 736 patients compared 12.5 and 25 mg of rofecoxib once daily with 800 mg of ibuprofen 3 times daily, and a 1-year study compared 12.5 and 25 mg of rofecoxib once daily with 50 mg of diclofenac 3 times daily in 693 patients.

Results: Rofecoxib, at 12.5 and 25 mg, demonstrated efficacy clinically comparable with ibuprofen, assessed by 3 primary end points according to predefined comparability criteria. Both rofecoxib doses and ibuprofen provided significantly greater efficacy than placebo on all primary end points at 6 weeks. Both rofecoxib doses and diclofenac showed similar efficacy over 1 year. All treatments were well tolerated.

Conclusions: Rofecoxib is effective in treating OA with once-daily dosing for 6 weeks and 1 year. Rofecoxib was generally safe and well-tolerated in OA patients for 6 weeks and 1 year. Arch Fam Med. 2000;9:1124-1134

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Rofecoxib是一种新的环氧化酶2抑制剂,在骨关节炎患者的6周和1年的试验中显示出与其他非甾体类抗炎药相当的持续疗效。骨关节炎研究组。
Rofecoxib是一种环氧化酶2抑制剂(有时被称为特异性环氧化酶2抑制剂或Coxib),用于骨关节炎(OA)。已发表的信息表明,罗非昔布比非选择性非甾体抗炎药(NSAIDs)具有更好的胃肠道安全性。目的:评价罗非昔布治疗骨性关节炎的疗效和安全性。方法:采用相同的入组标准和终点,对膝关节或髋关节OA患者进行两项随机、双盲、平行组研究。在一项为期6周的安慰剂对照试验中,736名患者将12.5和25毫克罗非昔布每日1次与800毫克布洛芬每日3次进行了比较,在一项为期1年的研究中,693名患者将12.5和25毫克罗非昔布每日1次与50毫克双氯芬酸每日3次进行了比较。结果:罗非昔布12.5 mg和25 mg的疗效与布洛芬具有临床可比性,根据预先确定的可比性标准通过3个主要终点进行评估。在6周的所有主要终点上,罗非昔布和布洛芬的疗效都明显高于安慰剂。罗非昔布和双氯芬酸在1年内的疗效相似。所有治疗均耐受良好。结论:罗非昔布治疗OA有效,每日1次,疗程6周1年。罗非昔布在OA患者6周和1年内总体上是安全且耐受性良好的。中华医学杂志。2000;9:1104 - 1104
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