Product image of Kabazitaksel Fresenius Kabi (Cabazitaxel) supplied by GNH India

Kabazitaksel Fresenius Kabi

Active Ingredient:
Cabazitaxel
Origin:
EU

Kabazitaksel Fresenius Kabi (Cabazitaxel)

Cabazitaxel, the active ingredient in Kabazitaksel Fresenius Kabi, is a taxane presented as an injectable solution for intravenous use. It is indicated for metastatic castration‑resistant prostate cancer after prior docetaxel therapy.

GNH India supplies Kabazitaksel Fresenius Kabi as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide.

Manufacturer / TM Owner

Fresenius Kabi D.O.O.

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Indications & Clinical Uses

  • Kabazitaksel is a taxane chemotherapy used in the treatment pathway of advanced prostate cancer.
  • Metastatic castration‑resistant prostate cancer: provides a therapeutic option after docetaxel failure, improving disease control and overall survival.

How It Works

  • Cabazitaxel binds to the β‑tubulin subunit of microtubules, promoting polymerization and stabilizing the microtubule network. This prevents depolymerization, disrupts mitotic spindle formation, arrests cell division in the G2/M phase, and triggers apoptotic pathways in rapidly dividing cancer cells.

Side Effects

Cabazitaxel is associated with 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.
  • Anemia: lowered red blood cells causing weakness.
  • Nausea and vomiting: gastrointestinal upset.
  • Diarrhea: loose stools that may lead to dehydration.
  • Alopecia: hair loss on scalp and body.

Serious or Rare Side Effects

  • Febrile neutropenia: fever with low neutrophils requiring urgent care.
  • Severe hypersensitivity reactions: rash, bronchospasm, or anaphylaxis.
  • Life‑threatening infections: sepsis or opportunistic infections.
  • Pulmonary toxicity: interstitial pneumonitis or fibrosis.
  • Peripheral neuropathy: numbness or tingling in extremities.
  • Cardiac events: arrhythmias or myocardial ischemia.

Precautions & Warnings

  • Before initiating therapy, clinicians should assess patient-specific risk factors and monitor for toxicity.
  • Monitor blood counts: perform regular CBC to detect neutropenia.
  • Assess liver function: evaluate hepatic enzymes as cabazitaxel is hepatically cleared.
  • Evaluate for hypersensitivity: observe for infusion‑related reactions during administration.
  • Avoid in severe infection: postpone dosing until infection resolves.
  • Use with caution in the elderly: consider dose adjustments based on tolerance.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Cabazitaxel may interact with other medicines that affect its metabolism or increase toxicity.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): can raise cabazitaxel plasma levels.
  • Potent CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce efficacy.
  • Concurrent myelosuppressive agents: increase risk of severe neutropenia.

Moderate Interactions (Monitor Closely)

  • P‑glycoprotein inhibitors (e.g., verapamil): may modestly increase exposure.
  • Anticoagulants (e.g., warfarin): heightened bleeding risk due to platelet effects.
  • CYP2C8 substrates (e.g., paclitaxel): potential additive toxicity.

Frequently Asked Questions

Kabazitaksel contains cabazitaxel, a taxane chemotherapy indicated for patients with metastatic castration‑resistant prostate cancer who have progressed after prior docetaxel therapy. It is used to slow disease progression and extend survival in this specific patient population.

Cabazitaxel binds to β‑tubulin, promoting microtubule polymerization and preventing depolymerization. This stabilizes the microtubule network, blocks mitotic spindle formation, arrests cells in the G2/M phase, and ultimately triggers apoptosis of rapidly dividing cancer cells.

The dosing regimen for Kabazitaksel is determined by the prescribing oncologist based on individual patient factors such as body surface area, prior therapies, and laboratory values. Healthcare professionals set the exact dose and schedule.

Cabazitaxel is classified as contraindicated in pregnancy because it can cause fetal harm. It is also not recommended for breastfeeding mothers, as it may be excreted in milk and affect the infant. Women of childbearing potential should use effective contraception.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying 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.

Kabazitaksel (cabazitaxel) is a second‑generation taxane designed to overcome resistance to first‑generation agents like docetaxel. It has a higher affinity for tubulin and retains activity in tumors that have become resistant to docetaxel, offering an alternative when disease progresses after initial taxane therapy.

Kabazitaksel must be stored refrigerated at 2‑8 °C, protected from light, and should never be frozen or shaken. The product should be kept in its original packaging until preparation for intravenous infusion.

Kabazitaksel is given as an intravenous infusion. The solution is prepared according to the manufacturer’s instructions and administered by a qualified healthcare professional, typically over a period of 30–60 minutes, with appropriate pre‑medication to reduce infusion‑related reactions.

The most serious risks include febrile neutropenia, severe infections, hypersensitivity reactions, pulmonary toxicity, and life‑threatening cardiac events. Patients should be closely monitored for signs of infection, respiratory distress, and cardiac abnormalities throughout treatment.

Kabazitaksel should not be used in patients with known hypersensitivity to cabazitaxel or any of its excipients, in those with uncontrolled severe infections, or in individuals with significant hepatic impairment where dose adjustment is not feasible. Caution is also advised for patients with pre‑existing cardiac disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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