Results from a phase 3 comparison trial have indicated that prescription chondroitin sulphate is as effective as the anti-inflammatory drug celecoxib in treating patients with osteoarthritis (OA) of the knee. The randomized, double-blind, double-dummy ChONdroitin vs. Celecoxib vs. Placebo Trial (CONCEPT) enrolled a total of 604 patients in five European countries.
The study’s primary objective was to determine the efficacy and safety of prescription chondroitin sulphate in comparison with that of placebo during six months of treatment, with celecoxib as an active comparator.
The study involved male and female outpatients, 50 years of age or older, with primary knee OA of the medial or latero-femoro-tibial compartment, as defined by American College of Rheumatology (ACR) criteria. The patients were randomly assigned to receive one 800-mg capsule of chondroitin (Condosulf, IBSA) plus one tablet of celecoxib placebo; one tablet of chondroitin placebo plus one 200-mg capsule of celecoxib; or one tablet of chondroitin placebo and one tablet of celecoxib placebo once daily for 182 days. Paracetamol 500 mg was available as a rescue medication (a maximum of six tablets). The study’s coprimary endpoints consisted of a decrease in Lequesne algo-functional index scores and a decrease in visual analog scale (VAS) pain scores. A total of 505 patients completed the study: 160 in the chondroitin group, 172 in the placebo group, and 173 in the celecoxib group.
Baseline Huskisson’s VAS pain scores were 70.6 for the chondroitin group, 69.9 for the placebo group, and 69.7 for celecoxib group. At month 6, the respective VAS scores were 33.6, 40.8, and 33.6. The difference between chondroitin and placebo was statistically significant (P < 0.05).
Lequesne scores at baseline were 11.7 for the chondroitin group, 11.8 for the placebo group, and 11.5 for the celecoxib group. At month 6, the respective scores were 7.5, 8.5, and 7.3. Again, the difference between chondroitin and placebo was statistically significant (P < 0.05).
The safety population consisted of 199 chondroitin-treated patients, 205 placebo-treated patients, and 200 celecoxib-treated patients. Adverse events occurred in 100 (50%), 110 (54%), and 103 (52%) patients in these respective groups. The between-group differences were not statistically significant. Twenty-two (11%), 12 (6%), and 19 (10%) patients in the chondroitin, placebo, and celecoxib groups, respectively, experienced adverse drug reactions, mainly gastrointestinal in nature.
The investigators concluded that:
Sources: PR Newswire; June 13, 2016; and IBSA; June 8, 2016.