Overview

52 Week, International, Multi-center, Randomized, Double-blind, Double-dummy, Parallel-group Clinical Trial to Compare Retention on Treatment, Safety, Tolerability & Efficacy of Lumiracoxib 100 mg od, Lumiracoxib 100 mg Bid & Celecoxib 200 mg od in

Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
Participant gender:
Summary
This trial will compare the retention on treatment (based on the rate of patients staying on treatment for 1 year) of patients suffering from primary osteoarthritis using two different doses of lumiracoxib (100 mg od or 100 mg bid) or using celecoxib (200 mg od)
Phase:
Phase 3
Details
Lead Sponsor:
Novartis
Treatments:
Celecoxib
Diclofenac
Lumiracoxib