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Clinical Trial Summary

In the STOP-UVEITIS study, we propose to evaluate the safety, tolerability, and bioactivity of two doses of Tocilizumab (4mg/kg and 8mg/kg), administered monthly, in patients with non-infectious intermediate, posterior, or panuveitis.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01717170
Study type Interventional
Source University of Nebraska
Contact
Status Active, not recruiting
Phase Phase 1/Phase 2
Start date March 2013
Completion date December 2017

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