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A Study to Compare the Pharmacokinetics of BR4002 and BR4002-1 in Healthy Volunteers

Dementia Alzheimers Clinical Trial

Official title:
A Randomized, Open-label, Single-dose, Crossover Study to Evaluate the Pharmacokinetics and Safety/Tolerability of BR4002 Comparing to BR4002-1 in Healthy Volunteers

Clinical Trial Summary

This study is designed as a randomized, open-label, single-dose, 6x3 crossover study.

Clinical Trial Description

A total of 18 subjects will be randomized into 6 sequence groups. The investigational products will be administered according to the treatment groups (R, T1, and T2) assigned to each sequence group in Period 1, Period 2, and Period 3. In between each period, there will be a washout period (28 days) long enough for the administered IP to be metabolized and eliminated. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04462029
Study type Interventional
Source Boryung Pharmaceutical Co., Ltd
Contact
Status Completed
Phase Early Phase 1
Start date June 5, 2020
Completion date October 7, 2020
View Details
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