drugset / Trial / NCT00152425

Study to Test the Effect of CDP870 in the Treatment of Crohn's Disease Over 26 Weeks, Comparing CDP870 to a Dummy Drug (Placebo), Following 3 Doses of Active Drug (CDP870).

NCT00152425 ↗

Phase 3 Completed 392 enrolled UCB Pharma
RandomizedParallel-groupDouble-blind

Summary

A 26 week maintenance study of CDP870 in Crohn's disease

Timeline

Start
2004-02
Primary completion
2005-05
Completion
2005-05

Outcome

Met primary endpoint

paper the primary end point) who were receiving certolizumab pegol (vs. 34% of those receiving placebo, P<0.001). PMID 17634459 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Certolizumab Pegol Protein / enzyme biologic 400 mg Subcutaneous

Indications