drugset / Trial / NCT00452140

Phase II Study With the Trifunctional Antibody Ertumaxomab to Treat Metastatic Breast Cancer Progressing After Endocrine Treatment

NCT00452140 ↗

Phase 2 Terminated 40 enrolled Neovii Biotech
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of the study is to demonstrate clinical efficacy of the investigational trifunctional bispecific antibody ertumaxomab for treatment of patients with HER-2/neu 1+ or 2+ (FISH-) expressing advanced or metastatic breast cancer (stage III b/IV) which has progressed after endocrine therapy. Ertumaxomab is a trifunctional bispecific antibody targeting Her-2/neu and CD3 on T cells. Trifunctional antibodies represent a new concept for targeted anticancer therapy. This new antibody class has the capability to redirect T cells and accessory cells (e.g. macrophages, dendritic cells \[DCs\] and natural killer \[NK\] cells) to the tumor site. According to preclinical data, trifunctional antibodies activate these immune cells, which can trigger a complex anti-tumor immune response.

Timeline

Start
2007-03
Primary completion
—
Completion
2009-02

Outcome

Outcome not reported

Stopped: “company focus on other projects”

Drugs

EvaluationDrugModalityDoseRoute
Subject ertumaxomab Monoclonal antibody 100 ug Intravenous

Indications