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Herzuma

Active Ingredient:
Trastuzumab
Origin:
EU

Herzuma (Trastuzumab)

Herzuma is a prescription intravenous solution that contains the monoclonal antibody trastuzumab as its active ingredient. It is supplied in a sterile liquid formulation for infusion and is marketed in the European Union. As a targeted antineoplastic agent, Herzuma is designed to bind the HER2 receptor on cancer cells, helping to inhibit tumor growth. The product is administered under the supervision of a qualified health‑care professional.

Manufacturer / TM Owner

Celltrion Healthcare Hungary Kft

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Indications & Clinical Uses

Herzuma is indicated for the treatment of several HER2‑positive malignancies. It is used in both metastatic and early‑stage disease settings as part of a prescribed therapeutic regimen.

  • HER2‑positive metastatic breast cancer
  • HER2‑positive early breast cancer (adjuvant or neoadjuvant)
  • HER2‑positive gastric adenocarcinoma
  • HER2‑positive gastro‑esophageal junction adenocarcinoma
  • Combination with chemotherapy in approved protocols

How It Works

  • Trastuzumab binds with high affinity to the extracellular domain IV of the human epidermal growth factor receptor 2 (HER2) protein expressed on the surface of certain cancer cells. This binding blocks ligand‑independent HER2 signaling, prevents receptor dimerization, and reduces downstream proliferative pathways such as PI3K/AKT and MAPK. Additionally, the Fc region of trastuzumab engages immune effector cells, triggering antibody‑dependent cellular cytotoxicity that contributes to tumor cell elimination.

Side Effects

Adverse reactions to Herzuma have been observed in clinical studies and post‑marketing experience. They can be grouped by frequency and severity.

Common

  • Infusion‑related reactions (fever, chills, flushing)
  • Nausea or vomiting
  • Fatigue
  • Headache

Serious

  • Cardiac dysfunction or decreased left ventricular ejection fraction
  • Severe hypersensitivity or anaphylaxis
  • Pulmonary toxicity (interstitial pneumonitis)
  • Thromboembolic events

Precautions & Warnings

Before initiating Herzuma, clinicians should evaluate patient history and monitor specific clinical parameters to reduce the risk of complications.

  • Assess baseline cardiac function (e.g., echocardiogram) and repeat periodically.
  • Review prior trastuzumab exposure or hypersensitivity reactions.
  • Monitor for signs of infusion‑related reactions during and after administration.
  • Use caution in patients with pre‑existing pulmonary disease.
  • Avoid use in pregnant women; discuss contraception and potential fetal risk.
  • Adjust treatment in patients with hepatic impairment as recommended.
  • Counsel patients on the importance of reporting new cardiac symptoms promptly.

Avoid Interactions

Herzuma may interact with other medicines that affect cardiac function or immune response. Relevant interactions are summarized below.

Avoid

  • Concurrent use with anthracyclines (e.g., doxorubicin) due to increased cardiotoxicity risk.
  • Live vaccines during treatment because of immunosuppression.

Use with caution

  • Other HER2‑targeted agents (pertuzumab, lapatinib) may increase toxicity.
  • Medications that prolong QT interval.
  • Drugs that cause significant hepatic enzyme induction or inhibition.

Frequently Asked Questions

Herzuma is a prescription monoclonal antibody formulated as an intravenous solution that contains the active ingredient trastuzumab.

Herzuma is used for HER2‑positive metastatic breast cancer, HER2‑positive early breast cancer, HER2‑positive gastric adenocarcinoma, and HER2‑positive gastro‑esophageal junction adenocarcinoma.

Trastuzumab binds to the extracellular domain of the HER2 receptor, blocking signaling pathways that promote cell growth and recruiting immune cells to destroy the tumor.

Yes, baseline and periodic assessment of left ventricular ejection fraction is recommended because trastuzumab can affect cardiac function.

Herzuma is often administered in combination with approved chemotherapy regimens as part of a treatment protocol for HER2‑positive cancers.

Common reactions include fever, chills, flushing, nausea, fatigue, and headache during or shortly after the infusion.

Serious events may include cardiac dysfunction, severe hypersensitivity or anaphylaxis, pulmonary toxicity, and thromboembolic complications.

Herzuma is not recommended during pregnancy; women of childbearing potential should use effective contraception and discuss risks with their health‑care provider.

Live vaccines should be avoided during treatment because trastuzumab can suppress the immune response.

Baseline cardiac imaging, liver function tests, and a review of prior trastuzumab exposure or hypersensitivity are typically performed.

Re‑treatment with trastuzumab‑based products may be considered, but clinicians should evaluate prior tolerance and cardiac status.

Herzuma itself is a biosimilar version of trastuzumab approved for use in the European Union.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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