GNH USA

Europe — EMA

Jevtana

GNH USA supplies Jevtana (cabazitaxel), a taxane antineoplastic agent for metastatic castration‑resistant prostate cancer after docetaxel therapy.

Cabazitaxel

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What is Cabazitaxel?

Cabazitaxel, the active ingredient in Jevtana, is a taxane presented as a 20 mg per vial injectable solution for intravenous use. It is indicated for metastatic castration‑resistant prostate cancer in patients whose disease has progressed after docetaxel chemotherapy.

GNH USA supplies Jevtana as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres, hospitals and pharmacies worldwide, complying with EU quality standards. The company provides regulated cold‑chain logistics and supports import documentation for global distribution. Clients benefit from consistent product quality, traceability and responsive technical support.

What is Cabazitaxel used for?

Cabazitaxel is a taxane chemotherapy used in the treatment pathway for advanced prostate cancer.

Metastatic castration‑resistant prostate cancer after docetaxel therapy: provides an additional line of therapy to improve disease control.

What are the side effects of Cabazitaxel?

Cabazitaxel may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects: - Neutropenia: reduced white blood cell count increasing infection risk. - Fatigue: persistent tiredness affecting daily activities. - Nausea: upset stomach often accompanied by vomiting. - Diarrhea: loose stools that may lead to dehydration.

Serious or Rare Side Effects: - Febrile neutropenia: fever with low neutrophils, a medical emergency. - Severe hypersensitivity reactions: rash, bronchospasm, or anaphylaxis. - Pulmonary embolism: blood clot in the lungs requiring urgent care. - Hepatic toxicity: elevated liver enzymes or liver failure. - Cardiac events: arrhythmias or myocardial infarction. - Severe diarrhea leading to electrolyte imbalance.

What precautions apply to Cabazitaxel?

Before initiating Jevtana therapy, clinicians should evaluate several safety considerations.

Pregnancy: Category D – avoid use unless benefits outweigh risks. Breastfeeding: not recommended due to potential drug excretion in milk. Renal impairment: assess kidney function and adjust monitoring. Hepatic impairment: consider dose modification and monitor liver enzymes. Concomitant myelosuppressive therapy: increase frequency of blood count monitoring. Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Cabazitaxel interact with?

Cabazitaxel can interact with other medicines, altering its efficacy or safety.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase cabazitaxel exposure. - Concurrent myelosuppressive agents: heightened risk of severe neutropenia. - Live vaccines: increased infection risk due to immunosuppression.

Moderate Interactions (Monitor Closely): - CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce therapeutic effect. - Anticoagulants: monitor for bleeding if thrombocytopenia occurs. - Diuretics: watch electrolyte balance during fluid shifts.

Frequently asked questions

What is Jevtana used for?+
Jevtana is the brand name for cabazitaxel, a taxane chemotherapy indicated for treatment of metastatic castration‑resistant prostate cancer in patients whose disease has progressed after prior docetaxel therapy. It is administered by intravenous infusion and provides an additional line of therapy aimed at slowing tumor growth.
How does cabazitaxel work?+
Cabazitaxel binds to tubulin subunits, promoting polymerization and stabilizing microtubules. This prevents the normal dynamic reorganization required for mitosis, leading to cell‑cycle arrest at the G2/M phase and ultimately triggering apoptosis of rapidly dividing cancer cells. Its activity is independent of common taxane resistance mechanisms.
What is the usual dose of Jevtana?+
The specific dose and infusion schedule of Jevtana are determined by the treating oncologist based on the patient’s clinical status, body surface area, and prior therapy. The prescribing information provides detailed guidance, and the prescriber tailors the regimen to achieve optimal efficacy while managing safety.
Is Jevtana safe during pregnancy or breastfeeding?+
Cabazitaxel is classified as Pregnancy Category D, indicating evidence of risk to the fetus. It should be avoided in pregnant women unless the potential benefit justifies the risk. Breastfeeding is not recommended because the drug may be excreted in milk and could harm the infant.
How do I order Jevtana from GNH USA?+
To place an order, 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 handling if needed—and assistance with import documentation.
How does Jevtana compare with other taxanes such as docetaxel?+
Both cabazitaxel and docetaxel belong to the taxane class and disrupt microtubule dynamics, but cabazitaxel has been designed to retain activity in tumors that have become resistant to docetaxel. Clinical studies show cabazitaxel can improve overall survival in patients who have progressed after docetaxel, though its safety profile includes a higher incidence of neutropenia.
What are the storage and handling requirements for Jevtana?+
Jevtana is supplied as a sterile injectable solution in 20 mg vials. It must be stored refrigerated at 2–8 °C, protected from light, and should not be frozen or shaken. Prior to infusion, the vial may be allowed to reach room temperature, but the solution must be used within the time frame specified in the label after reconstitution.
How is Jevtana administered?+
Jevtana is given by intravenous infusion, typically over a period of one hour, on a schedule determined by the oncologist (often every three weeks). The infusion is performed in a clinical setting where vital signs and blood counts can be monitored before, during, and after administration to manage potential adverse reactions.
What are the most serious risks associated with Jevtana?+
The most serious risks include severe neutropenia that can lead to infection, febrile neutropenia, hypersensitivity reactions, and rare but potentially fatal events such as pulmonary embolism or severe hepatic toxicity. Patients should be closely monitored for signs of infection, bleeding, liver dysfunction, and allergic responses throughout treatment.
Who should not receive Jevtana?+
Jevtana is contraindicated in patients with known hypersensitivity to cabazitaxel or any component of the formulation. It should also be avoided in individuals with uncontrolled infections, severe hepatic impairment, or those who are pregnant unless the therapeutic benefit outweighs the risk. Clinicians must assess each patient’s medical history before initiating therapy.
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
Cabazitaxel
Route
Intravenous Use
Manufacturer
Sanofi Winthrop Industrie
Origin
EU

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