drugset / Trial / NCT00674362
Rheumatoid Arthritis (RA) Moderate to Low Disease Activity Study
RandomizedParallel-groupQuadruple-blindTreatment
Summary
To assess the clinical efficacy and safety of certolizumab pegol as add-on therapy with stable-dose disease-modifying antirheumatic drugs (DMARDs) for achieving clinical remission in patients with moderate to low disease activity rheumatoid arthritis
Timeline
- Start
- 2008-06
- Primary completion
- 2010-05
- Completion
- 2010-12
Outcome
Met primary endpoint
paper Significantly more CZP patients met the primary endpoint than placebo patients (week 20 and 24 CDAI remission rates: 18.8% vs 6.1%; p≤0.05). PMID 24431394 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Certolizumab Pegol | Protein / enzyme biologic | 200 mg | Subcutaneous |