drugset / Trial / NCT03051217

A Study to Test the Efficacy and Safety of Certolizumab Pegol in Japanese Subjects With Moderate to Severe Chronic Psoriasis

NCT03051217 ↗

Phase 2/3 Completed 127 enrolled UCB Biopharma S.P.R.L.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to demonstrate the efficacy and safety of Certolizumab Pegol (CZP) in the treatment of moderate to severe chronic plaque Psoriasis (PSO) in Japanese subjects.

Timeline

Start
2017-02-21
Primary completion
2018-11-19
Completion
2019-01-16

Outcome

Met primary endpoint

registry Placebo (FAS) vs CZP 200 mg Q2W (FAS); p <0.0001; Odds Ratio (OR) 31.695 (97.5% CI 5.129 to 195.877); Regression, Logistic NCT03051217 ↗

registry Placebo (FAS) vs CZP 400 mg Q2W (FAS); p <0.0001; Odds Ratio (OR) 79.112 (97.5% CI 11.739 to 533.168); Regression, Logistic NCT03051217 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Certolizumab Pegol Protein / enzyme biologic 200 mg Subcutaneous
Subject Certolizumab Pegol Protein / enzyme biologic 400 mg Subcutaneous

Indications