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
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
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.