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Clinical Trial Summary

The primary objectives of this trial are (1) To show PK (Pharmacokinetic) similarity of BI 695500 to rituximab. (2)To establish statistical equivalence of efficacy of BI 695500 and rituximab, in patients with moderately to severely active RA (Rheumatoid Arthritis), based on the change in Disease Activity Score 28 (DAS28) score measured at 24 weeks compared to Baseline and the American College of Rheumatology 20% (ACR20) response rate at Week 24.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01682512
Study type Interventional
Source Boehringer Ingelheim
Contact
Status Terminated
Phase Phase 3
Start date September 5, 2012
Completion date October 12, 2016

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