Product image of Javlor (Vinflunine) supplied by GNH India

Javlor

Active Ingredient:
Vinflunine
Origin:
EU

Javlor (Vinflunine)

Vinflunine, the active ingredient in Javlor, is a Vinca alkaloid (microtubule inhibitor) presented as an intravenous solution for intravenous use. It is indicated for patients with advanced or metastatic urothelial carcinoma who have progressed after platinum‑based chemotherapy, offering a targeted antineoplastic option in later‑line treatment.

GNH India supplies Javlor as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide, with established cold‑chain logistics and regulatory support for cross‑border distribution. Our team ensures product integrity and timely delivery to meet clinical demand.

Manufacturer / TM Owner

Pierre Fabre Medicament

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Indications & Clinical Uses

  • Vinflunine is employed in the treatment of urothelial carcinoma, a cancer of the urinary tract.
  • Advanced or metastatic urothelial carcinoma: provides a therapeutic option after failure of platinum‑based chemotherapy to achieve disease control, potentially extending progression‑free survival and offering an additional line of therapy.
  • Platinum‑refractory urothelial carcinoma: serves as a later‑line treatment when standard platinum regimens are no longer effective, giving clinicians an alternative antineoplastic strategy.

How It Works

  • Vinflunine binds to tubulin at the vinca binding site, preventing microtubule polymerisation and destabilising the mitotic spindle. This inhibition of microtubule dynamics arrests cells in the G2/M phase of the cell cycle, leading to apoptosis of rapidly dividing cancer cells.

Side Effects

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

Common Side Effects

  • Neutropenia: reduced neutrophil count increasing infection risk.
  • Constipation: decreased bowel motility causing discomfort.
  • Nausea and vomiting: gastrointestinal upset often requiring anti‑emetics.
  • Fatigue: persistent tiredness affecting daily activities.
  • Alopecia: hair loss that may be temporary.

Serious or Rare Side Effects

  • Febrile neutropenia: fever with low neutrophils requiring urgent care.
  • Severe hemorrhage: bleeding complications due to platelet suppression.
  • Hepatic toxicity: elevated liver enzymes indicating liver injury.
  • Renal impairment: decreased kidney function necessitating monitoring.
  • Anaphylactic reactions: rare severe allergic responses needing immediate treatment.

Precautions & Warnings

  • Vinflunine requires careful monitoring and specific safety measures before and during therapy.
  • Monitor blood counts: perform regular complete blood counts to detect neutropenia or anemia.
  • Assess renal function: evaluate creatinine clearance prior to each infusion.
  • Evaluate hepatic function: check liver enzymes and bilirubin levels regularly.
  • Avoid use in severe neutropenia: do not administer if absolute neutrophil count is critically low.
  • Use with caution in elderly patients: consider dose adjustments and close observation.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake the solution.

Avoid Interactions

Vinflunine can interact with other medicines, altering its safety or effectiveness.

Major Interactions (Avoid)

  • Concurrent myelosuppressive chemotherapy: may exacerbate bone‑marrow suppression.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): increase vinflunine exposure and toxicity.
  • Live vaccines: heightened risk of infection due to immunosuppression.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce vinflunine plasma levels.
  • Antiemetics such as ondansetron: potential QT‑interval prolongation, monitor ECG.
  • Warfarin: possible alteration of INR, require regular coagulation monitoring.

Frequently Asked Questions

Javlor contains vinflunine and is used as a later‑line antineoplastic therapy for patients with advanced or metastatic urothelial carcinoma who have progressed after platinum‑based chemotherapy.

Vinflunine binds to tubulin at the vinca site, blocking microtubule polymerisation. This disrupts the mitotic spindle, arrests cells in the G2/M phase and triggers apoptosis of rapidly dividing cancer cells.

The dose of Javlor is determined by the prescribing oncologist based on the patient’s clinical condition, body surface area and laboratory parameters. Specific dosing regimens are not disclosed publicly.

Vinflunine is classified as contraindicated in pregnancy because it may cause fetal harm. It is also not recommended while breastfeeding, as it can be excreted in milk and affect the infant.

To request Javlor, 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 where needed) and necessary import documentation.

Javlor (vinflunine) is a microtubule inhibitor, differing from taxane‑based or immune‑checkpoint therapies. It offers an option after platinum failure, whereas alternatives may include immunotherapy or other chemotherapeutic agents, each with distinct efficacy and safety profiles.

Javlor must be stored at 2‑8 °C in a refrigerator, protected from light. The solution should not be frozen or shaken, and it should remain in its original packaging until ready for use.

Javlor is supplied as an intravenous solution that is infused by a qualified healthcare professional under controlled conditions, typically in an oncology infusion centre or hospital setting.

The most serious risks include febrile neutropenia, severe hemorrhage, hepatic toxicity, renal impairment and rare anaphylactic reactions. Patients should be closely monitored for signs of infection, bleeding, liver or kidney dysfunction.

Javlor should not be used in patients with severe baseline neutropenia, uncontrolled infections, significant hepatic or renal impairment, or in those who are pregnant. Contra‑indications are determined by the treating physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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