drugset / Trial / NCT03413319

Extension Study of ABBV-8E12 in Patients With Progressive Supranuclear Palsy (PSP) Who Completed Study C2N-8E12-WW-104

NCT03413319 ↗

Phase 1 Completed 3 enrolled AbbVie
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the long-term safety and tolerability of ABBV-8E12 in subjects with progressive supranuclear palsy (PSP).

Timeline

Start
2018-04-17
Primary completion
2019-11-20
Completion
2019-11-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Tilavonemab Monoclonal antibody — Intravenous