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Clinical Trial Summary

This study is a multi-center, open-label study of intravenous (IV) ANX005 in participants with ALS.


Clinical Trial Description

In this Phase 2a, multi-center, open label, proof-of-biology study, ANX005 will be administered to participants with ALS. The study consists of approximately 22 weeks of treatment and approximately 14 weeks of follow-up. All participants will be contacted by phone 6 months after study completion. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04569435
Study type Interventional
Source Annexon, Inc.
Contact Study Coordinator
Phone 650-822-5500
Email clinicaltrials@annexonbio.com
Status Recruiting
Phase Phase 2
Start date January 15, 2021
Completion date January 2024

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