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Clinical Trial Summary

The primary objectives of the study are to evaluate the effects of two doses of nalbuphine HCl ER tablets on the change from baseline in the worst itch Numerical Rating Scale (NRS) in patients with prurigo nodularis and to evaluate the safety and tolerability in the study population.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02174419
Study type Interventional
Source Trevi Therapeutics
Contact
Status Completed
Phase Phase 2/Phase 3
Start date March 2015
Completion date August 2016

See also
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