drugset / Trial / NCT02552212

Multicenter Study Evaluating Certolizumab Pegol Compared to Placebo in Subjects With axSpA Without X-ray Evidence of AS

NCT02552212 ↗

Phase 3 Completed 317 enrolled UCB BIOSCIENCES, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Patients with active Axial Spondyloarthritis without x-ray evidence of Ankylosing Spondylitis and with signs of inflammation will be randomly assigned to receive certolizumab pegol (CZP) 200 mg every two weeks or placebo. The primary objective is to demonstrate the efficacy of CZP in these patients.

Timeline

Start
2015-09
Primary completion
2018-05
Completion
2020-05

Outcome

Met primary endpoint

paper ASDAS-MI at week 52 was achieved in 47.2% (75 of 159) of CZP plus NBBM patients, which was significantly greater (P < 0.0001) PMID 30848558 ↗

registry analysis (other test); Placebo (FAS) vs CZP 200 mg Q2W (FAS); p <0.001; Odds Ratio (OR) 15.231 (95% CI 7.336 to 31.623) NCT02552212 ↗

registry NUMBER Placebo (FAS): 11.4 percentage of subjects NUMBER CZP 200 mg Q2W (FAS): 47.8 percentage of subjects NCT02552212 ↗

registry analysis (other test); Placebo (FAS) vs CZP 200 mg Q2W (FAS); p <0.001; Odds Ratio (OR) 7.436 (95% CI 4.127 to 13.401) NCT02552212 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Certolizumab Pegol Protein / enzyme biologic 200 mg Subcutaneous

Indications