drugset / Trial / NCT00686374

Efficacy and Long Term Safety of Adalimumab in Pediatric Subjects Who Have Demonstrated Clinical Response in M06-806

NCT00686374

Phase 3 Completed 100 enrolled AbbVie
NaSingle-groupOpen-labelTreatment

Summary

This was a multicenter, open-label study to evaluate the human monoclonal anti-TNF-α antibody adalimumab as an effective therapy for maintaining clinical response in pediatric participants with Crohn's disease (CD) and to gather long-term safety and tolerability data in this population. Participants were allowed to enroll in the study if they participated in and successfully completed Study M06-806 (NCT00409682) through Week 52.

Timeline

Start
2008-05-01
Primary completion
2017-04-04
Completion
2017-04-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Adalimumab Monoclonal antibody 10 mg Subcutaneous
Subject Adalimumab Monoclonal antibody 20 mg Subcutaneous
Subject Adalimumab Monoclonal antibody 40 mg Subcutaneous

Indications