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Clinical Trial Summary

This Phase 2 study was designed to evaluate the efficacy and safety of SNC-102 in subjects with drug-induced Tardive Dyskinesia (TD). To ensure an adequate evaluation of SNC-102, a randomized, double-blind, parallel-group, placebo-controlled trial was designed. Two dosing levels of SNC-102 are employed to evaluate the proposed dosing range. A target enrollment of 90 subjects with drug-induced TD will provide sufficient data to assess the efficacy and safety profiles of SNC-102 in the target population.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02064010
Study type Interventional
Source Synchroneuron Inc.
Contact
Status Withdrawn
Phase Phase 2
Start date February 2014
Completion date December 2015