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Bioavailability, Safety, and Tolerability of BIS-001 ER

Epilepsy, Complex Partial Clinical Trial

Official title:
Evaluation of the Bioavailability, Safety, and Tolerability of BIS-001 ER Following Multiple Dose Administration in Healthy Subjects

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

Clinical Trial Details
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
View Details
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