drugset / Trial / NCT02852694

Reduce Risk for Crohn's Disease Patients

NCT02852694

Phase 4 Completed 192 enrolled PIBD-Net European Commission · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to compare the effectiveness of weekly subcutaneously administered Methotrexate for maintaining relapse-free sustained steroid/Enteral Nutrition -free 1-year remission compared with: * daily oral Azathioprine / 6 mercaptopurine in low risk paediatric Crohn's disease * subcutaneously administered adalimumab in high risk paediatric Crohn's disease

Timeline

Start
2017-02-28
Primary completion
2021-06-14
Completion
2021-06-14

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Adalimumab Monoclonal antibody 40 mg Subcutaneous
Subject Adalimumab Monoclonal antibody 40 mg/m2 Subcutaneous
Comparator Azathioprine Small molecule 2.5 mg/kg Oral
Comparator MERCAPTOPURINE ANHYDROUS Small molecule 1.5 mg/kg Oral
Comparator Methotrexate Small molecule 15 mg/m2 Subcutaneous

Indications