Study of ANX005 in Adults With Amyotrophic Lateral Sclerosis (ALS)
NCT04569435 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 17
Last updated 2025-01-06
Summary
This study is a multi-center, open-label study of intravenous (IV) ANX005 in participants with ALS.
Conditions
Interventions
- DRUG
-
ANX005
IV Infusion
Sponsors & Collaborators
-
Annexon, Inc.
lead INDUSTRY
Principal Investigators
-
Benjamin Hoehn, MD, PhD · Annexon, Inc.
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-01-15
- Primary Completion
- 2024-01-10
- Completion
- 2024-04-23
- FDA Drug
- Yes
Countries
- United States
- Canada
Study Locations
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