drugset / Trial / NCT02137226

BI 695501 Compared to Adalimumab in Patients With Active Rheumatoid Arthritis

NCT02137226

Phase 3 Completed 645 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

Primary Objective: The primary objective of this trial is to establish an equivalence in efficacy between BI 695501 and US-licensed Humira® in patients with active Rheumatoid arthritis based on a statistical comparison of the proportion of patients meeting American College of Rheumatology 20% (ACR20) response rate at Week 12 and ACR20 response rate at Week 24 between BI 695501 and US-licensed Humira®. Secondary Objectives: The secondary objectives of this trial are to compare the efficacy, safety and immunogenicity of BI 695501 and US-licensed Humira® in patients with active RA including those undergoing the transition from US-licensed Humira® to BI 695501 after 24 weeks.

Timeline

Start
2015-01-26
Primary completion
2016-03-03
Completion
2016-10-18

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Adalimumab Monoclonal antibody
Subject BI 695501 Monoclonal antibody

Indications