Catumaxomab: clinical development and future directions

MAbs. 2010 Mar-Apr;2(2):129-36. doi: 10.4161/mabs.2.2.11221.

Abstract

Catumaxomab, a monoclonal bispecific trifunctional antibody, was approved in the European Union in April 2009 for the intraperitoneal treatment of patients with malignant ascites. The marketing authorization holder Fresenius Biotech GmbH developed catumaxomab (Removab(®)) together with its partner TRION Pharma GmbH, Germany. It is the first substance worldwide with a regulatory label for the treatment of malignant ascites due to epithelial carcinomas. Since the peritoneum is of mesothelial origin and therefore lacks EpCAM expression, the intraperitoneal administration of catumaxomab is an attractive targeted immunotherapeutic approach. Catumaxomab is able to destroy EpCAM positive tumor cells in the peritoneal cavity known as the main cause of malignant ascites. In addition, catumaxomab is a potential therapeutic option for several primary tumors since the EpCAM molecule is expressed on the majority of epithelial carcinomas. This review focuses on the clinical development of catumaxomab and indicates future directions.

Publication types

  • Review

MeSH terms

  • Animals
  • Antibodies, Bispecific / pharmacology*
  • Antibodies, Bispecific / therapeutic use
  • Antigens, Neoplasm / immunology
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / therapeutic use
  • Carcinoma / drug therapy*
  • Carcinoma / immunology
  • Carcinoma / pathology
  • Cell Adhesion Molecules / immunology
  • Drug Discovery
  • Epithelial Cell Adhesion Molecule
  • European Union
  • Humans
  • Immunomodulation
  • Immunotherapy* / trends
  • Peritoneal Neoplasms / drug therapy*
  • Peritoneal Neoplasms / immunology
  • Peritoneal Neoplasms / pathology

Substances

  • Antibodies, Bispecific
  • Antigens, Neoplasm
  • Antineoplastic Agents
  • Cell Adhesion Molecules
  • Epithelial Cell Adhesion Molecule
  • catumaxomab