drugset / Trial / NCT06335173

A Study to Evaluate Efficacy and Safety of Intravenous Sabirnetug in Participants With Early Alzheimer's Disease (ALTITUDE-AD)

NCT06335173

Phase 2 Active not recruiting 542 enrolled Acumen Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary purpose of this study is to evaluate the efficacy of sabirnetug infusions administered once every four weeks (Q4W) in slowing cognitive and functional decline as compared to placebo in participants with early Alzheimer's disease.

Timeline

Start
2024-02-29
Primary completion
2026-10
Completion
2026-10

Drugs

EvaluationDrugModalityDoseRoute
Subject sabirnetug Monoclonal antibody 35 mg/kg Intravenous
Subject sabirnetug Monoclonal antibody 50 mg/kg Intravenous

Indications