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 presented as an injectable solution for intravenous use. It is indicated for patients with advanced or metastatic urothelial carcinoma who have progressed after platinum‑based chemotherapy.

GNH India supplies Javlor as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Pierre Fabre Medicament

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Indications & Clinical Uses

Javlor is a Vinca alkaloid used in the treatment of urothelial carcinoma, a cancer of the bladder and urinary tract.

  • Advanced urothelial carcinoma: provides disease control after platinum‑based chemotherapy failure.
  • Metastatic urothelial carcinoma: offers a therapeutic option for patients with cancer spread beyond the bladder.
  • Urothelial carcinoma (post‑platinum): used to extend survival in patients whose disease has progressed following standard platinum regimens.

How It Works

  • Vinflunine binds to tubulin, inhibiting microtubule assembly and dynamics. This disruption interferes with mitotic spindle formation, leading to cell‑cycle arrest at the G2/M phase and ultimately triggering apoptosis in 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.
  • Anemia: lowered red blood cell levels causing fatigue.
  • Nausea and vomiting: gastrointestinal upset.
  • Constipation: decreased bowel movements.
  • Fatigue: general weakness and tiredness.
  • Alopecia: hair loss.

Serious or Rare Side Effects

  • Severe neutropenia with febrile infection.
  • Hemorrhage: bleeding complications.
  • Cardiac toxicity: arrhythmias or reduced cardiac function.
  • Severe hypersensitivity reactions: rash, bronchospasm, or anaphylaxis.
  • Renal failure: impaired kidney function.
  • Thromboembolic events: blood clots in veins or arteries.

Precautions & Warnings

Before initiating Vinflunine therapy, clinicians should assess patient-specific risk factors and monitor relevant parameters.

  • Blood count monitoring: perform regular CBC to detect myelosuppression.
  • Renal function assessment: evaluate creatinine clearance prior to each cycle.
  • Hepatic function assessment: check liver enzymes for potential toxicity.
  • Infection vigilance: avoid use in patients with active severe infections.
  • Cardiac caution: monitor ECG in patients with known heart disease.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

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

Major Interactions (Avoid)

  • Concurrent Vinca alkaloids or taxanes: additive neurotoxicity.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole): increase vinflunine exposure.
  • Potent CYP3A4 inducers (e.g., rifampicin): reduce therapeutic levels.
  • Nephrotoxic agents (e.g., cisplatin): heightened renal risk.
  • Anticoagulants (e.g., warfarin): increased bleeding tendency.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., erythromycin): may raise plasma concentrations.
  • Other myelosuppressive drugs (e.g., cyclophosphamide): enhanced bone‑marrow suppression.
  • CYP2C9 or CYP2C19 inhibitors: potential modest increase in exposure.
  • Diuretics: may affect renal clearance.
  • Proton‑pump inhibitors: possible alteration of absorption dynamics.

Frequently Asked Questions

Javlor contains vinflunine and is used to treat adults with advanced or metastatic urothelial carcinoma that has progressed after platinum‑based chemotherapy. It provides an additional line of therapy aimed at slowing disease progression and extending survival in this specific patient population.

Vinflunine interferes with microtubule dynamics by binding to tubulin, preventing proper spindle formation during cell division. This disruption halts the cell cycle at the G2/M checkpoint and triggers programmed cell death (apoptosis) in rapidly proliferating cancer cells, thereby reducing tumor growth.

The dosing regimen for Javlor is individualized by the prescribing oncologist based on factors such as patient weight, renal function, and prior treatment history. The prescriber determines the appropriate dose, infusion rate, and treatment schedule for each patient.

Safety data for vinflunine in pregnancy and lactation are limited. It is generally advised to avoid use during pregnancy unless the potential benefit justifies the risk to the fetus. Breastfeeding is not recommended while receiving treatment, as the drug may be excreted in milk.

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 if needed), and necessary import documentation.

Javlor (vinflunine) is a Vinca alkaloid distinct from taxanes or checkpoint inhibitors commonly used in urothelial carcinoma. It offers a chemotherapy option after platinum failure, with a different toxicity profile focused on myelosuppression and neutropenia, whereas immunotherapies target the immune system and may have immune‑related adverse events.

Javlor must be stored refrigerated at 2‑8 °C. Keep the vials in their original packaging, protect them from light, and do not freeze or shake the solution. If a short period at room temperature is unavoidable during preparation, use the product within the time frame specified by the manufacturer.

Javlor is supplied as an injectable solution for intravenous infusion. It is administered by a qualified healthcare professional, typically over a set period (e.g., 30‑60 minutes) according to the prescriber's instructions and institutional protocols.

The most serious risks include severe neutropenia leading to infection, hemorrhage, cardiac toxicity, and rare but life‑threatening hypersensitivity reactions. Patients should be closely monitored for signs of infection, bleeding, cardiac events, and allergic responses throughout treatment.

Javlor is contraindicated in patients with known hypersensitivity to vinflunine or any component of the formulation. It should also be avoided in individuals with uncontrolled severe infections, significant cardiac disease, or severe renal impairment unless dose adjustments are made and benefits outweigh risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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