A Study of AMDX-2011P in Participants With CAA

Status Recruiting

Clinical Trial Summary

The purpose of this study is to assess safety, tolerability, plasma pharmacokinetics and biologic activity of a single intravenous dose of AMDX-2011P in participants with cerebral amyloid angiopathy (CAA).

Clinical Trial Description

This open-label, masked endpoint assessment study will evaluate the safety, tolerability, plasma pharmacokinetics (PK) and biological activity of an intravenous (IV) dose of AMDX-2011P in participants with CAA. Assessments of retinal images will be conducted by central masked assessors. Participants will be admitted to the study site where eye examination and retinal imaging will be conducted before administration of the study drug. AMDX-2011P will be administered through a single IV bolus injection followed by safety assessments, retinal imaging and PK blood collection. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05709314
Study type	Interventional
Source	Amydis Inc.
Contact	Joyce Simpauco, MPH
Phone	858-254-7435
Email	joyce@amydis.com
Status	Recruiting
Phase	Phase 2
Start date	April 2024
Completion date	December 2024

View Details

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