CIMZIA is indicated for the treatment of adults with moderately to severely active rheumatoid arthritis (RA).
In clinical trials with CIMZIA, a majority of patients experienced a significant reduction of the signs and symptoms of RA and significant inhibition of structural damage at weeks 24 and 52, with some patients experiencing a reduction in symptoms within 1 to 2 weeks.1,2
In the 52-week RAPID 1 pivotal clinical trial with CIMZIA, a co-primary end point was ACR20 response rate at week 24 (59% vs 14% for placebo).1 Significant ACR20 response to CIMZIA was seen as early as 1 to 2 weeks in some patients, peaking at week 12 in 64% of patients.1,2