drugset / Trial / NCT02460094

Multiple Ascending Dose Study of Intravenously Administered BMS-986168 (BIIB092) in Patients With Progressive Supranuclear Palsy

NCT02460094 ↗

Phase 1 Completed 48 enrolled Biogen
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to evaluate the safety and tolerability of multiple ascending intravenous infusions of BMS-986168 and to assess the pharmacokinetics and immunogenicity of BIIB092, and pharmacodynamics of BIIB092 on cerebrospinal fluid (CSF) extracellular tau (eTau) concentrations in participants with Progressive Supranuclear Palsy.

Timeline

Start
2015-10-02
Primary completion
2016-10-19
Completion
2016-10-19

Drugs

EvaluationDrugModalityDoseRoute
Subject gosuranemab Monoclonal antibody 150 mg Intravenous
Subject gosuranemab Monoclonal antibody 700 mg Intravenous
Subject gosuranemab Monoclonal antibody 2100 mg Intravenous