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Clinical Trial Summary

The purpose of this research study is to assess the ability of AMDX- 2011P to identify amyloid deposits in the retina of participants with Primary Open Angle Glaucoma (POAG).


Clinical Trial Description

This open-label, masked endpoint assessment study will evaluate safety, tolerability, plasma pharmacokinetics (PK) and biological activity of intravenous (IV) doses of AMDX-2011P in participants with POAG. Assessments of retinal images will be conducted by centrally 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 blood collection and PK. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06223048
Study type Interventional
Source Amydis Inc.
Contact Joyce Simpauco
Phone 858-254-7435
Email joyce@amydis.com
Status Recruiting
Phase Phase 2
Start date December 7, 2023
Completion date July 2024

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