drugset / Trial / NCT01284062
Pharmacokinetics/Pharmacodynamics Biomarker Study in Active Ulcerative Colitis Patients
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Anrukinzumab | Monoclonal antibody | 200 mg | Intravenous |
| Subject | Anrukinzumab | Monoclonal antibody | 400 mg | Intravenous |
| Subject | Anrukinzumab | Monoclonal antibody | 600 mg | Intravenous |