drugset / Trial / NCT02065570

Study to Evaluate Efficacy and Safety of Two Drug Regimens in Subjects With Moderate to Severe Crohn's Disease

NCT02065570

Phase 3 Completed 514 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will evaluate higher versus standard adalimumab dosing regimens for induction and maintenance therapy in subjects with moderately to severely active Crohn's Disease and evidence of mucosal ulceration.

Timeline

Start
2014-05-01
Primary completion
2020-01-30
Completion
2020-01-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Adalimumab Monoclonal antibody 40 mg
Subject Adalimumab Monoclonal antibody 80 mg
Subject Adalimumab Monoclonal antibody 160 mg

Indications