Overview

A Study to Evaluate ALN-5288 in Patients With Alzheimer's Disease

Status:
NOT_YET_RECRUITING
Trial end date:
2030-03-31
Target enrollment:
Participant gender:
Summary
The purpose of this study is to: * Evaluate the safety and tolerability of intrathecal (IT) ALN-5288 in patients with Alzheimer's Disease (AD) * Evaluate the pharmacodynamic (PD) and pharmacokinetic (PK) effects of ALN-5288 after dose administration
Phase:
PHASE1
Details
Lead Sponsor:
Alnylam Pharmaceuticals
Collaborator:
Regeneron Pharmaceuticals