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Clinical Trial Summary

The primary objective of this study is to evaluate the safety and tolerability of a range of single and 13 repeated doses of BIIB054, administered as intravenous (IV) infusion, in Japanese participants with Parkinson's disease (PD). The secondary objectives are to evaluate the immunogenicity, and serum pharmacokinetics (PK) profile of BIIB054 after single and multiple dose administration.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03716570
Study type Interventional
Source Biogen
Contact
Status Terminated
Phase Phase 1
Start date March 12, 2019
Completion date April 23, 2021

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