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Clinical Trial Summary

This Phase 3, multi-center study will evaluate the long-term safety and tolerability of hydrocodone bitartrate controlled release capsule (HC-CR) at daily doses of 40 mg or more in subjects with moderate to severe chronic pain. Long-term maintenance of HC-CR efficacy will be evaluated.


Clinical Trial Description

Subjects will go through screening, an open-label conversion and titration phase of up to 6 weeks followed by an open-label treatment phase for up to 48 weeks with a 2 week follow-up period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01115569
Study type Interventional
Source UCB Pharma
Contact
Status Completed
Phase Phase 3
Start date May 2010
Completion date January 2012

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