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Clinical Trial 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.


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


NCT number NCT02658916
Study type Interventional
Source Biogen
Contact
Status Terminated
Phase Phase 1
Start date February 22, 2016
Completion date March 31, 2020

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