drugset / Trial / NCT02880956

A Study to Evaluate the Efficacy and Safety of ABBV-8E12 in Participants With Early Alzheimer's Disease

NCT02880956 ↗

Phase 2 Completed 453 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study seeks to evaluate the efficacy and safety of ABBV-8E12 in participants with early Alzheimer's disease (AD).

Timeline

Start
2017-01-26
Primary completion
2021-03-30
Completion
2021-07-28

Outcome

Missed primary endpoint

registry analysis (superiority test); Placebo vs ABBV-8E12 300 mg; p = 0.740; Least Squares (LS) Mean of Difference 0.06 (95% CI -0.291 to 0.409) NCT02880956 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Tilavonemab Monoclonal antibody 300 mg Intravenous
Subject Tilavonemab Monoclonal antibody 1000 mg Intravenous
Subject Tilavonemab Monoclonal antibody 2000 mg Intravenous

Indications