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

NCT04569435 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 17

Last updated 2025-01-06

No results posted yet for this study

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

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04569435 on ClinicalTrials.gov