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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


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

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