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A Study to Evaluate the Pharmacokinetics and Safety of BEY2153 in Healthy Participants

Alzheimer's Disease Clinical Trial

Official title:
A Randomized, Double-blind, Placebo-controlled, Single and Multiple Ascending Dose Phase I Clinical Trial to Evaluate the Safety, Tolerability and Pharmacokinetics of BEY2153 After Oral Administration in Healthy Young and Elderly Male Volunteers.

Clinical Trial Summary

This is a first in human Phase 1 study to evaluate the safety, tolerability and pharmacokinetics with healthy young and elderly adult male volunteers after receiving single and multiple ascending dose of BEY2153.

Clinical Trial Description

Healthy young and elderly adult volunteers who meet the criteria, will be treated single and multiple ascending dose of BEY2153 or placebo orally. Food effect evaluation study will be conducted with single ascending dose. After the single ascending dose study, independent external experts will review blinded data and multiple ascending dose study will be conducted. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04476303
Study type Interventional
Source BeyondBio Inc.
Contact
Status Recruiting
Phase Phase 1
Start date August 28, 2020
Completion date October 2021
View Details
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