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Clinical Trial Summary

This is a single dose, dose-escalation study to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of TB006, a monoclonal antibody that will be studied as a disease modifying treatment for Alzheimer's disease.


Clinical Trial Description

The TB006 nonclinical pharmacology program establishes its potential as a therapeutic agent for AD. Overall, the data suggest the potential for beneficial therapeutic effects of TB006 in addressing underlying pathology and ameliorating the course of AD. The preclinical safety profile of TB006 further supports the clinical investigation of TB006. This is a Phase 1 SAD study in healthy adult subjects. The study will evaluate the safety, tolerability, and PK of single doses of TB006, administered as an IV infusion over 1 hour. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04920786
Study type Interventional
Source TrueBinding, Inc.
Contact Anna Cabral
Phone 714-891-0971
Email annecabral@cnstrial.com
Status Recruiting
Phase Phase 1
Start date June 1, 2021
Completion date January 1, 2023

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