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Clinical Trial Summary

This study is intended to evaluate the efficacy and safety of ANX005 administered by intravenous (IV) infusion to participants recently diagnosed with Guillain-Barré Syndrome (GBS). The total duration of study participation is approximately 6 months.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04701164
Study type Interventional
Source Annexon, Inc.
Contact Study Coordinator
Phone 650-822-5500
Email clinicaltrials@annexonbio.com
Status Recruiting
Phase Phase 3
Start date December 17, 2020
Completion date April 30, 2024

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