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Clinical Trial Summary

Investigate the efficacy and safety of DS-5565 in subjects with Post-Herpetic Neuralgia (PHN) in comparison to placebo


Clinical Trial Description

[Double Blind Phase] The primary objective is to compare change in the Average Daily Pain Score (ADPS) from baseline to Week 14 in Asian subjects with PHN receiving DS-5565 versus placebo. [Open Extension Phase] The objective is to assess the long-term safety and efficacy of DS-5565 in subjects with PHN. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02318719
Study type Interventional
Source Daiichi Sankyo, Inc.
Contact
Status Completed
Phase N/A
Start date January 2015
Completion date May 25, 2017

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