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

Citation
K. Saag et al., 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, ARCH FAM M, 9(10), 2000, pp. 1124-1134
Citations number
33
Categorie Soggetti
General & Internal Medicine
Journal title
ARCHIVES OF FAMILY MEDICINE
ISSN journal
10633987 → ACNP
Volume
9
Issue
10
Year of publication
2000
Pages
1124 - 1134
Database
ISI
SICI code
1063-3987(200011/12)9:10<1124:RANC2I>2.0.ZU;2-G
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 (NSA IDs). 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 w ith 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 com parable with ibuprofen, assessed by 3 primary end points according to prede fined comparability criteria. Both rofecoxib doses and ibuprofen provided s ignificantly greater efficacy than placebo on all primary end points at 6 w eeks. Both rofecoxib doses and diclofenac showed similar efficacy over 1 ye ar. All treatments were well tolerated. Conclusions: Rofecoxib is effective in treating OA with once-daily dosing f or 6 weeks and 1 year. Rofecoxib was generally safe and well-tolerated in O A patients for 6 weeks and 1 year.