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RECRUITING
NCT07020819
PHASE3

An Open Label Clinical Study to Evaluate Tanruprubart (Also Commonly Known as ANX005) in Participants With Guillain-Barré Syndrome (FORWARD Study)

Sponsor: Annexon, Inc.

View on ClinicalTrials.gov

Summary

The goal of this open label study is to measure pharmacokinetics, pharmacodynamics, early efficacy, and safety of tanruprubart in adult and pediatric participants, in the United States, Canada, and Europe.

Official title: An Open-Label Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Efficacy, and Safety of a Single Dose of Tanruprubart (Also Commonly Known as ANX005) in Participants With Guillain-Barré Syndrome (GBS) (FORWARD Study)

Key Details

Gender

All

Age Range

12 Years - 85 Years

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2025-09-12

Completion Date

2028-06-30

Last Updated

2026-02-20

Healthy Volunteers

No

Interventions

DRUG

Tanruprubart

Solution for IV infusion.

Locations (9)

HonorHealth Bob Bové Neuroscience Institute

Scottsdale, Arizona, United States

Children's Hospital of Orange County

Orange, California, United States

University of California Irvine

Orange, California, United States

University of Colorado Hospital

Aurora, Colorado, United States

Ochsner LSU Health

Shreveport, Louisiana, United States

University Massachusetts Chan Medical School

Worcester, Massachusetts, United States

Henry Ford Health

Detroit, Michigan, United States

Mayo Rochester

Rochester, Minnesota, United States

Aarhus University Hospital

Aarhus, Aarhus N, Denmark