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Clinical Trial Summary

The primary objective is to evaluate the safety and tolerability of single ascending dose of Y-2 sublingual tablets in healthy male and female adult subjects. The secondary objective is to characterize the single-dose pharmacokinetics of Y-2 sublingual tablets in healthy male and female adult subjects.


Clinical Trial Description

This study will be a single-center, single ascending dose study in healthy male and female subjects. A total of 24 subjects, 4 cohorts of 6 subjects each, will be enrolled in this study. All of the 6 subjects in each cohort will receive a single dose of Y-2 sublingual tablet on a single occasion. Prior to taking the drug and after taking the drug at 5 min to 24 h, venous blood from all subjects will be collected at different time points for PK analysis. After dosing, safety and tolerability data for each cohort will be evaluated. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03495206
Study type Interventional
Source Yantai YenePharma Co., Ltd.
Contact David Z. Wang, M.D.
Phone (309) 624-9500
Email david.wang@chinastroke.net
Status Not yet recruiting
Phase Phase 1
Start date April 2018
Completion date October 2018

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