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Multiple Ascending Dose Study of Intravenously Administered BMS-986168 (BIIB092) in Patients With Progressive Supranuclear Palsy — CN002-003  

Progressive Supranuclear Palsy Clinical Trial

Official title:
A Randomized, Double-Blind, Placebo-Controlled, Multiple Ascending Dose Study of Intravenously Administered BMS-986168 in Patients With Progressive Supranuclear Palsy

Clinical Trial 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.

Clinical Trial Description

This study, previously posted by Bristol-Myers Squibb, has transitioned to Biogen under a licensing agreement. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02460094
Study type Interventional
Source Biogen
Contact
Status Completed
Phase Phase 1
Start date October 2, 2015
Completion date October 19, 2016
View Details
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