drugset / Trial / NCT02880956
A Study to Evaluate the Efficacy and Safety of ABBV-8E12 in Participants With Early Alzheimer's Disease
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Tilavonemab | Monoclonal antibody | 300 mg | Intravenous |
| Subject | Tilavonemab | Monoclonal antibody | 1000 mg | Intravenous |
| Subject | Tilavonemab | Monoclonal antibody | 2000 mg | Intravenous |