Product image of Hertraz 440 (Trastuzumab) 440 mg Vials supplied by GNH India

Hertraz 440

Active Ingredient:
Trastuzumab
Form:
Vials
Brand:
Hertraz
Origin:
India

Hertraz 440 (Trastuzumab Vials) 440 mg

Trastuzumab, the active ingredient in Hertraz 440, is a monoclonal antibody presented as a 440mg vial for intravenous infusion. It targets the HER2 protein found on some cancer cells and is used to treat HER2-positive breast cancer and HER2-positive metastatic gastric cancer, given alone or with chemotherapy after HER2 testing confirms the target. GNH India supplies Hertraz 440 as a licensed, GDP-compliant international pharmaceutical supplier serving oncology centres worldwide.

Strength

440 mg

Pack Size

1s

Storage

2-8°

Manufacturer / TM Owner

Biocon Biologics India Limited

1
Pack/s
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Indications & Clinical Uses

Trastuzumab is used to treat cancers that overexpress the HER2 protein, confirmed by laboratory testing before treatment.

  • Early HER2-positive breast cancer: given after surgery, and sometimes before it, to lower the risk of the cancer returning.
  • Metastatic HER2-positive breast cancer: treats advanced disease, alone or combined with chemotherapy.
  • HER2-positive metastatic gastric cancer: treats advanced stomach or gastro-oesophageal junction cancer with chemotherapy in patients not previously treated.
  • Combination with chemotherapy: often used alongside taxane or other regimens to improve response in suitable patients.

How It Works

  • Trastuzumab targets HER2, a receptor protein that sits on the surface of some breast and stomach cancer cells and drives them to grow and divide. By binding to HER2, trastuzumab blocks the growth signals these cancers depend on and slows or stops their proliferation. It also flags the cancer cells for destruction by the immune system. Because it acts on HER2-positive cells, healthy tissue without this target is largely spared.

Side Effects

Report any new symptom during treatment, especially breathlessness, cough, or ankle swelling, which may signal heart or lung effects.

Common Side Effects

  • Fever, chills, and infusion reactions: common, especially with the first infusion.
  • Nausea, vomiting, and diarrhoea: frequent digestive effects during treatment.
  • Fatigue, headache, and muscle pain: general effects across treatment cycles.
  • Low blood counts: reduced white cells or platelets, particularly with chemotherapy.

Serious or Rare Side Effects

  • Heart failure and reduced heart function: trastuzumab can weaken the heart, more so with anthracycline chemotherapy; report breathlessness, swelling, or a fast heartbeat.
  • Serious infusion reactions: severe reactions including anaphylaxis; stop the infusion and seek emergency care for breathing difficulty or collapse.
  • Lung toxicity and harm in pregnancy: seek urgent care for severe breathlessness, and use effective contraception, as it can seriously harm an unborn baby.

Precautions & Warnings

Trastuzumab needs careful cardiac monitoring and patient selection before and during treatment.

  • Check heart function first: measure heart pump function before starting, monitor it during treatment, and stop for significant decline.
  • Confirm HER2 status: treat only patients whose cancer tests positive for HER2 overexpression.
  • Take extra care with anthracyclines: combined use raises the risk of heart damage, so monitor closely.
  • Monitor for infusion reactions: watch during and after infusions and manage reactions promptly.
  • Prevent pregnancy: use effective contraception during treatment and for seven months after the last dose.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze, and use the prepared solution within the recommended time.

Avoid Interactions

Review trastuzumab against the patient’s other cancer treatments and heart medicines before each cycle.

Major Interactions (Avoid)

  • Anthracycline chemotherapy (doxorubicin, epirubicin): combined or recent use markedly raises the risk of heart failure, so monitor heart function closely.
  • Ado-trastuzumab emtansine: do not substitute or combine, as these are distinct products with different dosing.

Moderate Interactions (Monitor Closely)

  • Myelosuppressive chemotherapy: added bone marrow suppression can deepen low blood counts, so monitor counts.
  • Other cardiotoxic drugs: overlapping effects on the heart call for careful cardiac monitoring during treatment.
  • Live vaccines: use caution during treatment, particularly when trastuzumab is given alongside chemotherapy.

Frequently Asked Questions

Hertraz 440 contains trastuzumab, a targeted therapy for cancers that overexpress the HER2 protein. It is used to treat HER2-positive breast cancer, both early-stage after surgery and advanced disease, and HER2-positive metastatic stomach cancer. It is given alone or with chemotherapy, and only after a laboratory test confirms that the cancer is HER2-positive.

Trastuzumab attaches to HER2, a protein on the surface of some cancer cells that signals them to grow. By binding HER2, trastuzumab blocks these growth signals and slows or stops the cancer from multiplying. It also marks the cancer cells so the immune system can help destroy them. Because it targets HER2-positive cells, cells without this protein are largely unaffected.

Trastuzumab is dosed by body weight and set by the oncology team. A common schedule gives a higher loading dose followed by a maintenance dose every three weeks as an intravenous infusion, though a weekly schedule is also used. The 440mg multi-dose vial is reconstituted and the required amount drawn for each dose. Treatment length depends on the cancer and setting.

Yes. Trastuzumab can weaken the heart’s pumping function and, in some patients, cause heart failure, with the highest risk when it is combined with anthracycline chemotherapy. For this reason, heart function is checked before treatment and monitored during it. Any breathlessness, ankle swelling, or a fast or irregular heartbeat should be reported promptly so treatment can be reviewed.

You can request Hertraz 440 through the product page at gnhindia.com by submitting an enquiry with your required quantity. GNH India supplies hospitals, oncology centres, and procurement teams across international markets and will ask you to confirm trade or institutional credentials. The team then replies with pricing, availability, cold-chain shipping arrangements, and the documentation needed for import into your country.

Hertraz is a biosimilar of the original trastuzumab brand Herceptin, meaning it is a highly similar version of the same monoclonal antibody with no clinically meaningful differences in safety or effectiveness. Both target HER2-positive breast and gastric cancer and are used in the same way. A biosimilar allows access to trastuzumab therapy while meeting strict regulatory standards for quality and comparability.

Hertraz 440 vials should be kept refrigerated between 2 and 8°C in the original carton to protect them from light, and must not be frozen. The powder is reconstituted by a healthcare professional shortly before use. The reconstituted solution should be used within the recommended time, and any vial that looks discoloured or contains particles should be discarded.

Hertraz 440 is given as an intravenous infusion in a hospital or clinic, never as a rapid injection. The first infusion is given slowly and the patient watched closely for reactions; later infusions may be given over a shorter time if well tolerated. It is usually given every three weeks, and heart function is checked at regular intervals during treatment.

Trastuzumab can seriously harm an unborn baby, including reducing the fluid around the baby and affecting lung development, so it is avoided in pregnancy unless there is no safer option. Women who can become pregnant should use effective contraception during treatment and for seven months after the last dose. Anyone who becomes pregnant should tell their oncology team promptly.

Hertraz 440 should be avoided in anyone with a serious allergy to trastuzumab or its ingredients, and used with great caution in patients with existing heart problems or reduced heart function. It is only suitable for cancers confirmed as HER2-positive. An oncologist weighs the benefits against the cardiac and other risks and monitors the patient closely throughout.

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