drugset / Trial / NCT01284062

Pharmacokinetics/Pharmacodynamics Biomarker Study in Active Ulcerative Colitis Patients

NCT01284062 ↗

Phase 2 Completed 84 enrolled Pfizer
RandomizedParallel-groupTriple-blindTreatment

Summary

This study represents the first investigation of anrukinzumab in patients with active ulcerative colitis (UC) and will evaluate proof of mechanism by changes in the mechanism based biomarker (YKL 40) and pharmacodynamic biomarkers (fecal calprotectin, lactoferrin and hs-CRP). It will provide further assessment of the safety, tolerability, and pharmacokinetics (PK) by administration of multiple intravenous (IV) doses of anrukinzumab.

Timeline

Start
2011-03
Primary completion
2013-04
Completion
2013-04

Outcome

Missed primary endpoint

paper Fold change of FC from baseline at Week 14 was not significantly different for any treatment groups compared with the placebo. PMID 25567115 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Anrukinzumab Monoclonal antibody 200 mg Intravenous
Subject Anrukinzumab Monoclonal antibody 400 mg Intravenous
Subject Anrukinzumab Monoclonal antibody 600 mg Intravenous

Indications