Product image of Melphalan Zentiva (Melphalan Hydrochloride) supplied by GNH India

Melphalan Zentiva

Active Ingredient:
Melphalan Hydrochloride
Origin:
EU

Melphalan Zentiva (Melphalan Hydrochloride)

Melphalan, the active ingredient in Melphalan Zentiva, is a nitrogen‑mustard alkylating agent presented as an injectable solution for intravenous use. It is employed in the treatment of multiple myeloma, ovarian cancer, melanoma and other solid tumours in adult oncology patients.
GNH India supplies Melphalan Zentiva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Zentiva, K.S.

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Indications & Clinical Uses

  • Melphalan is an alkylating chemotherapy agent used in the treatment of various hematologic and solid tumors.
  • Multiple myeloma: reduces malignant plasma cells and prolongs survival.
  • Ovarian cancer: incorporated into combination regimens to target tumor growth.
  • Melanoma: administered as part of salvage therapy for advanced disease.
  • Other solid tumors: employed where alkylating agents are indicated to inhibit tumor proliferation.

How It Works

  • Melphalan exerts its antineoplastic effect by forming covalent cross‑links at the N7 position of guanine bases in DNA. This alkylation interferes with DNA replication and transcription, leading to strand breaks, inhibition of cell division, and ultimately apoptosis of rapidly dividing cancer cells.

Side Effects

Melphalan may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Nausea and vomiting
  • Myelosuppression (decreased white blood cells, red blood cells, and platelets)
  • Mucositis (inflammation of the mouth lining)
  • Fatigue or general weakness

Serious or Rare Side Effects

  • Secondary malignancies such as therapy‑related leukemia
  • Severe pulmonary toxicity (interstitial pneumonitis)
  • Renal impairment or acute kidney injury
  • Life‑threatening infections due to profound neutropenia

Precautions & Warnings

  • Before initiating therapy, clinicians should evaluate patient‑specific risk factors and monitor laboratory parameters closely.
  • Baseline blood counts: obtain complete blood count and differential.
  • Renal function assessment: check serum creatinine and calculate clearance.
  • Hepatic function: evaluate liver enzymes and bilirubin levels.
  • Pregnancy and lactation: avoid use unless benefits clearly outweigh risks.
  • Concomitant myelosuppressive agents: adjust dosing or increase monitoring frequency.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Melphalan can interact with other drugs, altering its efficacy or toxicity profile.

Major Interactions (Avoid)

  • Concurrent use of other alkylating agents: may increase cumulative bone‑marrow suppression.
  • Strong CYP450 inducers (e.g., rifampin): may reduce plasma concentrations.
  • High‑dose radiotherapy: synergistic toxicity to normal tissues.

Moderate Interactions (Monitor Closely)

  • Antiemetics (e.g., ondansetron): may affect melphalan clearance.
  • Nephrotoxic drugs (e.g., cisplatin, aminoglycosides): increase risk of renal injury.
  • Anticoagulants (e.g., warfarin): monitor coagulation parameters due to potential platelet count changes.

Frequently Asked Questions

Melphalan Zentiva is used in oncology to treat multiple myeloma, ovarian cancer, melanoma and other solid tumours where an alkylating chemotherapy agent is indicated.

Melphalan alkylates the N7 position of guanine in DNA, creating cross‑links that prevent DNA replication and transcription, which leads to cell cycle arrest and death of rapidly dividing cancer cells.

The dose of Melphalan Zentiva is individualized by the prescribing oncologist based on the specific indication, patient weight, renal function and treatment protocol.

Melphalan is classified as contraindicated in pregnancy and breastfeeding because it can cause fetal harm and is excreted in breast milk; it should only be used if the potential benefit justifies the risk.

Submit an enquiry on the product page at gnhindia.com with 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 and import documentation.

Melphalan shares the same DNA‑cross‑linking mechanism as other nitrogen‑mustard agents but differs in its pharmacokinetic profile and approved indications, offering a therapeutic option especially in multiple myeloma and certain solid tumours.

Melphalan Zentiva should be stored at 2‑8 °C, protected from light, and kept in its original container. Do not freeze or shake the product.

Melphalan Zentiva is administered intravenously by a qualified healthcare professional, typically as an infusion over a specified period according to the treatment protocol.

The most serious risks include severe myelosuppression leading to infection or bleeding, secondary malignancies such as therapy‑related leukemia, and organ toxicities like pulmonary fibrosis or renal impairment.

Patients with known hypersensitivity to melphalan or other nitrogen‑mustard agents, those with severe bone‑marrow failure, uncontrolled infections, or significant renal/hepatic dysfunction should not receive Melphalan Zentiva.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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