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Clinical Trial Summary

The goal of this Phase 2 MCI study is to determine whether 1.0 mg/kg XPro1595 is superior to placebo at improving measures of cognition, functioning and brain quality in individuals with MCI and biomarkers associated with neuroinflammation (APOE4) and to evaluate safety, tolerability, and efficacy of XPro1595.


Clinical Trial Description

This study is designed as a Phase 2, double-blind randomized, placebo-controlled study investigating the safety, tolerability, and efficacy of XPro1595 in patients with MCI. The planned dose is 1.0 mg/kg of XPro1595 and matching placebo. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05321498
Study type Interventional
Source Inmune Bio, Inc.
Contact
Status Withdrawn
Phase Phase 2
Start date June 2023
Completion date October 26, 2023

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