Product image of Korjuny (Catumaxomab) supplied by GNH India

Korjuny

Active Ingredient:
Catumaxomab
Origin:
EU

Korjuny (Catumaxomab)

Catumaxomab, the active ingredient in Korjuny, is a monoclonal antibody (bispecific) presented as a sterile solution for intraperitoneal use. It is employed to manage malignant ascites associated with EpCAM‑positive peritoneal carcinomatosis in adult cancer patients by facilitating immune‑mediated tumor cell destruction.

GNH India supplies Korjuny as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres, hospitals and specialty pharmacies worldwide. The company adheres to stringent quality standards and provides regulatory documentation for global distribution.

Manufacturer / TM Owner

Atnahs Pharma Netherlands B.V.

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Indications & Clinical Uses

Korjuny is indicated for malignant ascites associated with EpCAM‑positive peritoneal carcinomatosis, a condition within the peritoneal cancer disease family.

  • Malignant ascites: reduces fluid accumulation and improves patient comfort.
  • Peritoneal carcinomatosis: targets and eliminates EpCAM‑expressing tumor cells within the peritoneal cavity.
  • Quality of life: helps control symptoms related to ascitic buildup in affected patients.

How It Works

  • Catumaxomab is a bispecific monoclonal antibody that simultaneously binds EpCAM on tumor cells and CD3 on T lymphocytes. This dual binding creates an immunological synapse, activating T cells and triggering cytokine release, which leads to targeted tumor cell lysis and clearance from the peritoneal cavity.

Side Effects

Common Side Effects

  • Fever: transient elevation of body temperature after administration.
  • Abdominal pain: discomfort localized to the peritoneal area.
  • Nausea and vomiting: gastrointestinal upset occurring shortly after dosing.
  • Fatigue: generalized tiredness experienced during the treatment course.

Serious or Rare Side Effects

  • Cytokine release syndrome: severe systemic inflammatory response requiring medical intervention.
  • Hypotension: significant drop in blood pressure that may need monitoring.
  • Severe allergic reactions: including anaphylaxis, urticaria or angioedema.

Precautions & Warnings

Precautions should be observed when using Korjuny to minimize risks and ensure optimal therapeutic outcomes.

  • Cytokine release monitoring: observe patients for signs of systemic inflammation during and after infusion.
  • Liver function assessment: evaluate hepatic enzymes before and during therapy.
  • Immunosuppression caution: avoid use in patients with severe immunodeficiency.
  • Cardiac disease awareness: monitor cardiovascular status in patients with pre‑existing heart conditions.
  • Pregnancy and lactation: safety not established; use only if clearly needed.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Potential drug interactions must be considered to avoid compromising safety or efficacy.

Major Interactions (Avoid)

  • Concurrent immunomodulatory antibodies: may increase risk of severe immune reactions.
  • Live vaccines: contraindicated due to immunosuppressive effects.
  • High‑dose corticosteroids: can diminish therapeutic activity.

Moderate Interactions (Monitor Closely)

  • Cytotoxic chemotherapy agents: monitor for additive toxicity.
  • Antibiotics affecting gut flora: may alter infection risk.
  • Anticoagulants: observe for bleeding tendencies.

Frequently Asked Questions

Korjuny is used to treat malignant ascites that develop in patients with EpCAM‑positive peritoneal carcinomatosis. By targeting tumor cells within the peritoneal cavity, it helps reduce fluid buildup and improves symptom control.

Catumaxomab is a bispecific antibody that binds EpCAM on cancer cells and CD3 on T‑cells. This dual binding activates T‑cells, leading to cytokine release and direct destruction of the targeted tumor cells in the peritoneal space.

The dose of Korjuny is determined by the prescribing physician based on the patient’s clinical condition, body weight, and treatment protocol. Specific dosing regimens are not disclosed publicly.

Safety data for catumaxomab in pregnancy or lactation are limited. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision must be made by the treating physician.

To order Korjuny, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and import documentation.

Korjuny is a targeted immunotherapy that directly engages the patient’s immune system, whereas conventional options such as repeated paracentesis or systemic chemotherapy provide symptomatic relief without specific tumor targeting. Its bispecific mechanism offers a distinct therapeutic approach compared with non‑specific agents.

Korjuny must be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the product. Keep it in the original packaging until ready for use to maintain stability.

Korjuny is given as an intraperitoneal infusion. The medication is introduced directly into the peritoneal cavity under aseptic conditions, typically by a qualified healthcare professional in a clinical setting.

The most serious risks include cytokine release syndrome, severe hypotension, and life‑threatening allergic reactions such as anaphylaxis. Patients should be closely monitored during and after infusion for any signs of these events.

Korjuny should not be used in patients with known hypersensitivity to catumaxomab or any of its excipients, in those with severe immunosuppression, or in individuals receiving live vaccines. Contra‑indications are determined by the treating physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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