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Clinical Trial Summary

Primary Objective:

The primary objective of this trial is to compare the clinical efficacy of BI 695501 with EU-approved Humira® in patients with active Crohn's disease (CD).

Secondary Objectives:

The secondary objectives of this trial are to compare the efficacy and safety of BI 695501 with EU-approved Humira® across the induction and maintenance phases.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02871635
Study type Interventional
Source Boehringer Ingelheim
Contact
Status Completed
Phase Phase 3
Start date September 28, 2016
Completion date May 13, 2019

See also
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