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Clinical Trial Summary

The primary purpose of the study is to evaluate the change from baseline after 4 weeks of topical administration of TV-45070 (4% and 8% ointment) compared with placebo for the relief of symptoms of primary OA affecting a single knee


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02068599
Study type Interventional
Source Teva Branded Pharmaceutical Products R&D, Inc.
Contact
Status Completed
Phase Phase 2
Start date April 14, 2014
Completion date May 4, 2015

See also
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