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Catumaxomab - Lindis Biotech

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Drug Profile

Catumaxomab - Lindis Biotech

Alternative Names: Anti-CD3 anti-EpCAM monoclonal antibody; Anti-EpCAM anti-CD3 monoclonal antibody; KORJUNY; LP-000; Removab

Latest Information Update: 27 Feb 2025

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At a glance

  • Originator Lindis Biotech
  • Developer Lindis Biotech; Linton Pharm; Neovii Biotech; TRION Pharma
  • Class Antineoplastics; Bispecific antibodies; Immunoglobulin Fc fragments; Immunotherapies
  • Mechanism of Action Antibody-dependent cell cytotoxicity; Cytotoxic T lymphocyte stimulants
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    Yes - Gastric cancer; Ovarian cancer
  • New Molecular Entity Yes
  • Available For Licensing Yes

Highest Development Phases

  • Registered Malignant ascites
  • Phase III Gastric cancer
  • Phase I/II Bladder cancer
  • Discontinued Carcinoma; Ovarian cancer

Most Recent Events

  • 10 Feb 2025 Registered for Malignant ascites in European Union, Iceland, Liechtenstein, Norway (Intraperitoneal) - First global approval
  • 19 Nov 2024 EU marketing authorization is anticipated by the end of 2024
  • 19 Nov 2024 Catumaxomab licensed to Pharmanovia in Europe

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