drugset / Trial / NCT03391765
An Extension Study of ABBV-8E12 in Progressive Supranuclear Palsy (PSP)
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The purpose of this study was to assess the long-term safety and efficacy of ABBV-8E12 (tilavonemab) in participants with progressive supranuclear palsy (PSP).
Timeline
- Start
- 2018-01-24
- Primary completion
- 2019-12-13
- Completion
- 2019-12-13
Outcome
Outcome not reported
Stopped: “This study was prematurely discontinued because the program for progressive supranuclear palsy was discontinued due to lack of efficacy.”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Tilavonemab | Monoclonal antibody | 2000 mg | Intravenous |
| Subject | Tilavonemab | Monoclonal antibody | 4000 mg | Intravenous |