drugset / Trial / NCT03156439

Bioavailability, Safety, and Tolerability of BIS-001 ER

NCT03156439

NaSingle-groupOpen-labelTreatment

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.

Timeline

Start
2017-05-22
Primary completion
2017-09-30
Completion
2017-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Huperzine A Traditional medicine (herbal / TCM) 2.5 mg