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Clinical Trial Summary

This study investigates the safety, tolerability, and pharmacokinetics of BIS-001 ER in healthy volunteers. Subjects will be dosed twice daily, with a dose escalation occurring every 2-3 days until a maximum dose of 5mg per day is reached.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03156439
Study type Interventional
Source Biscayne Neurotherapeutics, Inc.
Contact
Status Completed
Phase Phase 1
Start date May 22, 2017
Completion date September 30, 2017

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