drugset / Trial / NCT02658916

Extension Study of BIIB092 in Participants With Progressive Supranuclear Palsy (PSP) Who Participated in CN002003

NCT02658916 ↗

Phase 1 Terminated 47 enrolled Biogen
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the long-term safety and tolerability of multiple intravenous (IV) infusions of BIIB092 in participants with Progressive Supranuclear Palsy (PSP). The study will also assess the pharmacodynamic (PD) effects of BIIB092 on cerebrospinal fluid (CSF) N-terminal tau, pharmacokinetics (PK), and immunogenicity of BIIB092 in participants with PSP.

Timeline

Start
2016-02-22
Primary completion
2020-03-31
Completion
2020-03-31

Outcome

Outcome not reported

Stopped: “251PP301(NCT03068468) primary endpoint was not met;further development of Gosuranemab BIIB092 in progressive supranuclear palsy will not be pursued.”

Drugs

EvaluationDrugModalityDoseRoute
Subject gosuranemab Monoclonal antibody — Intravenous