drugset / Trial / NCT01502423

A Crossover Study of the Safety and Tolerability of Two Formulations of Adalimumab

NCT01502423

Phase 2 Completed 61 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 three countries, Australia (3 sites), Canada (2 sites), and Germany (2 sites).

Timeline

Start
2012-01
Primary completion
2012-11
Completion
2012-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Adalimumab Monoclonal antibody 40 mg Subcutaneous

Indications