GNH USA

Europe — EMA

Kadcyla

GNH USA supplies Kadcyla (Trastuzumab emtansine), an antibody‑drug conjugate for HER2‑positive breast cancer and gastric adenocarcinoma. Request a quote.

Trastuzumab Emtansine

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What is Trastuzumab Emtansine?

Trastuzumab emtansine, the active ingredient in Kadcyla, is an antibody‑drug conjugate presented as a sterile powder for reconstitution for intravenous injection. It is indicated for the treatment of HER2‑positive metastatic breast cancer and HER2‑positive gastric or gastro‑esophageal junction adenocarcinoma in adult patients.

GNH USA supplies Kadcyla as a licensed, GDP‑compliant international pharmaceutical supplier, providing the product to oncology centres, hospitals and pharmacies worldwide under strict quality standards and regulatory compliance. The company ensures reliable cold‑chain logistics and supports clinical teams with documentation for import and distribution.

What is Trastuzumab Emtansine used for?

Kadcyla is used in HER2‑targeted therapy for certain advanced cancers.

- Metastatic HER2‑positive breast cancer: improves overall survival and disease control. - HER2‑positive gastric adenocarcinoma: provides clinical benefit in previously treated patients. - HER2‑positive gastro‑esophageal junction adenocarcinoma: extends progression‑free interval in advanced disease.

What are the side effects of Trastuzumab Emtansine?

Common Side Effects: - Fatigue: persistent tiredness reported by many patients. - Nausea: mild to moderate gastrointestinal upset. - Thrombocytopenia: reduced platelet counts requiring monitoring. - Anemia: decreased red blood cell levels causing weakness. - Elevated liver enzymes: transient increases in ALT/AST. - Alopecia: hair thinning or loss during treatment.

Serious or Rare Side Effects: - Interstitial lung disease: breathing difficulties that may be life‑threatening. - Cardiac dysfunction: reduced left ventricular ejection fraction. - Severe hepatic toxicity: marked elevation of liver enzymes or hepatitis. - Hemorrhage: significant bleeding events. - Infusion‑related reactions: fever, chills, or hypotension during administration.

What precautions apply to Trastuzumab Emtansine?

Kadcyla requires careful monitoring and specific safety measures.

- Cardiac monitoring: assess left ventricular ejection fraction before and during treatment. - Hepatic function: monitor liver enzymes regularly. - Bleeding risk: evaluate platelet counts and avoid concomitant anticoagulants if possible. - Pregnancy and lactation: avoid use; discuss risks with physician. - Infusion reactions: administer premedication and monitor during infusion. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Trastuzumab Emtansine interact with?

Kadcyla may interact with other medicines; some combinations should be avoided while others need close observation.

Major Interactions (Avoid): - Concurrent anthracyclines: increased cardiotoxicity. - Strong CYP3A4 inhibitors: may increase exposure to the cytotoxic payload. - Live vaccines: risk of infection due to immunosuppression.

Moderate Interactions (Monitor Closely): - Anticoagulants: increased bleeding risk. - Other HER2‑targeted agents: additive toxicity. - Hepatotoxic drugs: monitor liver function closely.

Frequently asked questions

What conditions is Kadcyla used to treat?+
Kadcyla is indicated for adult patients with HER2‑positive metastatic breast cancer and for HER2‑positive gastric or gastro‑esophageal junction adenocarcinoma that has progressed after prior therapy. It is part of HER2‑targeted treatment strategies in oncology.
How does trastuzumab emtansine work in the body?+
Trastuzumab emtansine combines a monoclonal antibody that binds HER2 receptors with the cytotoxic agent DM1. After binding to HER2‑expressing cancer cells, the complex is internalized, releasing DM1, which disrupts microtubules, causing cell‑cycle arrest and apoptosis while the antibody blocks HER2 signaling.
What is the usual dose of Kadcyla?+
The prescribed dose of Kadcyla is determined by the treating oncologist based on the patient’s clinical condition, body weight, and treatment protocol. Dosing regimens are individualized and should follow the prescribing information provided by the healthcare professional.
Is Kadcyla safe to use during pregnancy or while breastfeeding?+
Kadcyla’s safety in pregnancy and lactation has not been established. It is generally contraindicated in pregnant or nursing women because of potential risks to the fetus or infant. Women of child‑bearing potential should use effective contraception during treatment and for a defined period afterward.
How do I order Kadcyla from GNH USA?+
To order Kadcyla, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain logistics) and necessary import documentation.
How does Kadcyla compare with other HER2‑targeted therapies?+
Kadcyla differs from other HER2‑targeted agents such as trastuzumab alone because it delivers a cytotoxic payload (DM1) directly to HER2‑expressing cells, providing both antibody‑mediated inhibition and chemotherapy. This dual mechanism can offer benefit in patients who have progressed on standard HER2 therapies.
What are the storage and handling requirements for Kadcyla?+
Kadcyla must be stored refrigerated at 2 °C to 8 °C. It should be kept in its original packaging, protected from light, and must not be frozen or shaken. Once prepared for infusion, the solution should be used within the time frame specified in the product labeling.
How is Kadcyla administered to patients?+
Kadcyla is given as an intravenous infusion. The drug is supplied as a sterile powder that is reconstituted and diluted according to the prescribing information, then infused over a period of typically 30 to 90 minutes under medical supervision.
What are the most serious risks associated with Kadcyla?+
Serious risks include interstitial lung disease or pneumonitis, cardiac dysfunction (reduced left ventricular ejection fraction), severe hepatic toxicity, significant bleeding, and infusion‑related reactions. Patients should be monitored closely for symptoms of these conditions throughout treatment.
Who should not receive Kadcyla?+
Kadcyla is contraindicated in patients with known hypersensitivity to trastuzumab, emtansine, or any component of the formulation. It should also be avoided in individuals with uncontrolled cardiac disease, active severe infections, or those who are pregnant or breastfeeding.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Trastuzumab Emtansine
Route
Intravenous Use
Manufacturer
Roche Registration Gmbh
Origin
EU

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