NCT03133988

Brief Summary

The purpose of the Expanded Access program is to provide margetuximab to patients with pretreated HER2+ breast cancer for whom potential benefit justifies potential treatment risks.

Trial Health

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 20, 2017

Completed
8 days until next milestone

First Posted

Study publicly available on registry

April 28, 2017

Completed
Last Updated

February 14, 2025

Status Verified

February 1, 2025

First QC Date

April 20, 2017

Last Update Submit

February 12, 2025

Conditions

Interventions

MargetuximabBIOLOGICAL

anti-HER2 monoclonal antibody

Also known as: MGAH22

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • TerSera may consider requests on a case-by-case basis from treating physicians for patients not otherwise eligible for margetuximab clinical studies.
  • Treating physicians should consider approved therapies for a patient's disease, as well as ongoing clinical studies, before seeking expanded access use with an investigational agent.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

margetuximab

Study Design

Study Type
expanded access
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 20, 2017

First Posted

April 28, 2017

Last Updated

February 14, 2025

Record last verified: 2025-02