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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |