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Catumaxomab

ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS

Also known as: korjuny

EMA approvedATC L01FX03

Data last refreshed: (DrugCentral release 2024-11-01)

Key facts

Catumaxomab is a drug catalogued in DrugCentral. It was first approved by the EMA in 2025. DrugCentral lists 1 molecular target, including EPCAM. Recorded indications include Malignant ascites in adults with EpCAM-positive epithelial carcinomas.

  • Molecular targets: EPCAM (1 listed in DrugCentral).
  • Indications: Malignant ascites in adults with EpCAM-positive epithelial carcinomas.
  • ATC code: L01FX03 (Other monoclonal antibodies and antibody drug conjugates).

Indications & contraindications

Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).

Indications (1)

  • Malignant ascites in adults with EpCAM-positive epithelial carcinomas

Mechanism & targets

Molecular targets (1)

TargetGeneActionActivity
Epithelial cell adhesion moleculeEPCAMother—

Regulatory approvals (1)

DateAgencyMarketed asApplicantOrphan
2025-02-10EMA—Atnahs Pharma Netherlands B.V.

ATC classification

ATC codeTherapeutic hierarchy
L01FX03ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS › ANTINEOPLASTIC AGENTS › MONOCLONAL ANTIBODIES AND ANTIBODY DRUG CONJUGATES › Other monoclonal antibodies and antibody drug conjugates

Chemical structure

Molecular formula—
Molecular weight—
CAS number—
InChIKey—
PubChem CID—

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

What is Catumaxomab used for?

DrugCentral lists the following indications for Catumaxomab: Malignant ascites in adults with EpCAM-positive epithelial carcinomas.

How does Catumaxomab work?

Its molecular targets in DrugCentral include EPCAM.

When was Catumaxomab first approved?

Catumaxomab was first approved by the EMA in 2025.

Browse: all drugs starting with C · drug guides by category · protein targets A–Z.

Sources

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For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

Quick facts

Status—
First approval2025-02-10
AgencyEMA
Targets1
Indications1
Formula—
DrugCentral ID5853
Interactive profile