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Clinical Trial Summary

Double-blind, crossover, randomized, 3x3 Latin square, placebo-controlled study of single intravenous dose administration of VVZ-149. To demonstrate assay sensitivity, lidocaine will be administered as a positive control. The study will take place during a single inpatient visit involving three separate treatment periods, each with a washout of (>16-hours. Study drugs (VVZ-149 vs. lidocaine vs. normal saline, NS) will be administered intravenously.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02644421
Study type Interventional
Source Brigham and Women's Hospital
Contact
Status Completed
Phase Phase 1
Start date November 2015
Completion date July 2017

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