Study of ANX005 in Adults With Amyotrophic Lateral Sclerosis (ALS)

Status Recruiting

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

Clinical Trial Details

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

View Details

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