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Clinical Trial Summary

This is an open-study with a 26 week open label treatment period followed by an optional 26 week open label extension. The total treatment period will be 52 weeks.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02082197
Study type Interventional
Source AbbVie
Contact
Status Withdrawn
Phase Phase 3
Start date March 2014
Completion date June 2015

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