drugset / Trial / NCT01561313

Crossover Study of Safety and Tolerability of Two Formulations of Adalimumab.

NCT01561313

Phase 2 Completed 64 enrolled AbbVie
RandomizedCrossoverSingle-blindTreatment

Summary

This study will compare injection site pain levels between current Humira® formulation versus a new formulation of Humira in patients with Rheumatoid Arthritis (RA), who are either currently on a stable dose (minimum six consecutive doses) of on-label Humira or biological naïve who will be prescribed on-label Humira as treatment for their Rheumatoid Arthritis. The study is being conducted in two countries, Belgium (3 sites) and the Czech Republic (3 sites).

Timeline

Start
2012-03
Primary completion
2012-11
Completion
2012-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Adalimumab Monoclonal antibody 40 mg Subcutaneous

Indications