drugset / Trial / NCT04971733

A Study to Assess Safety and Target Engagement of E2814 in Participants With Mild to Moderate Cognitive Impairment Due to Dominantly Inherited Alzheimer's Disease

NCT04971733

Phase 1/2 Completed 8 enrolled Eisai Inc.
NaSequentialOpen-labelTreatment

Summary

The primary objective of the study is to assess the safety and tolerability of intravenous (IV) infusions of E2814 in participants with dominantly inherited Alzheimer's disease (DIAD), and to evaluate target engagement (TE) of E2814 on microtubule binding region (MTBR)-tau species in cerebrospinal fluid (CSF) in participants with DIAD.

Timeline

Start
2021-06-28
Primary completion
2024-05-24
Completion
2024-05-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Etalanetug Monoclonal antibody 750 mg Intravenous
Subject Etalanetug Monoclonal antibody 1500 mg Intravenous
Subject Etalanetug Monoclonal antibody 3000 mg Intravenous
Subject Etalanetug Monoclonal antibody 4500 mg Intravenous

Indications