NCT04278235

Brief Summary

This is an expanded access program (EAP) for eligible participants. This program is designed to provide access to Elezanumab prior to approval by the local regulatory agency. Availability will depend on territory eligibility. A medical doctor must decide whether the potential benefit outweighs the risk of receiving an investigational therapy based on the individual patient's medical history and program eligibility criteria.

Trial Health

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 18, 2020

Completed
2 days until next milestone

First Posted

Study publicly available on registry

February 20, 2020

Completed
Last Updated

February 3, 2026

Status Verified

April 1, 2025

First QC Date

February 18, 2020

Last Update Submit

January 30, 2026

Conditions

Acute Spinal Cord Injury (SCI)

Keywords

Expanded AccessPre-approval AccessCompassionate UseSpecial Access ProgramNamed Patient BasisSpecial Access Scheme

Interventions

ElezanumabDRUG

Solution for intravenous (IV) infusion

Also known as: ABT-555

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may not qualify if:

  • There are other suitable treatment options.
  • The participant qualifies for ongoing clinical trials.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

elezanumab

Study Officials

  • ABBVIE INC.

    AbbVie

    STUDY DIRECTOR

Central Study Contacts

ABBVIE CALL CENTER

CONTACT

844-663-3742abbvieclinicaltrials@abbvie.com

Study Design

Study Type
expanded access
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 18, 2020

First Posted

February 20, 2020

Last Updated

February 3, 2026

Record last verified: 2025-04