drugset / Trial / NCT06064864

Efficacy and Safety of Formulation Switching Between SC Infliximab and IV Infliximab in Patients With CD

NCT06064864

RandomizedCrossoverOpen-labelTreatment

Summary

The goal of this prospective, multicenter, open-label, randomized controlled, non-inferiority trial is to test efficacy and safety of formulation switching between subcutaneous (SC) infliximab and intravenous (IV) infliximab in patients with moderately to severely active Crohn's disease (CD). The primary endpoint of this study is deep remission at week 54. The main questions this study aims to answer are: Question-1) Is maintenance therapy with SC infliximab (120mg every 2 weeks) non-inferior to IV infliximab (5mg/kg every 8 weeks) in terms of deep remission at week 54? Question-2) Is maintenance therapy with SC infliximab (120mg every 2 weeks) non-inferior to IV infliximab (10mg/kg every 8 weeks) in terms of deep remission at week 54?

Timeline

Start
2023-10-09
Primary completion
2026-12-31
Completion
2026-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Infliximab Monoclonal antibody 5 mg/kg Subcutaneous
Subject Infliximab Monoclonal antibody 10 mg/kg Subcutaneous
Subject Infliximab Monoclonal antibody 120 mg Subcutaneous

Indications