drugset / Trial / NCT04006080

Investigation of the Faecal Loss of Vedolizumab and Its Role in Influencing Serum Drug Levels, Outcomes and Response in Ulcerative Colitis

NCT04006080

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to study the loss of vedolizumab in stool in patients with active ulcerative colitis (UC). Patients with moderate-to-severe UC who are commencing induction therapy with vedolizumab will be enrolled into a prospective study and stool will be collected for faecal vedolizumab measurement at days 1, 4 and 7; and again at weeks 2, 6 and 14. They will also be evaluated at three time-points (weeks 2, 6 and 14) for clinical and biochemical UC disease activity as well as serum vedolizumab concentrations and anti-vedolizumab antibodies.

Timeline

Start
2019-07-01
Primary completion
2020-03
Completion
2020-03

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Vedolizumab Monoclonal antibody Intravenous

Indications