Product image of Melphalan Macure (Melphalan) supplied by GNH India

Melphalan Macure

Active Ingredient:
Melphalan
Origin:
EU

Melphalan Macure (Melphalan)

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

Manufacturer / TM Owner

Macure Pharma Aps

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Indications & Clinical Uses

Melphalan is an alkylating chemotherapy used for several malignant disease groups.

  • Multiple myeloma: helps achieve disease control and prolong survival.
  • Ovarian cancer: used as part of combination regimens to reduce tumour burden.
  • Melanoma: administered to slow progression in advanced stages.
  • Other solid tumours: incorporated into protocols for selected refractory cancers.

How It Works

  • Melphalan exerts its antineoplastic effect by alkylating DNA bases, creating cross‑links that block DNA replication and transcription. The resulting DNA damage triggers cell‑cycle arrest and apoptosis, preferentially affecting rapidly dividing cancer cells while sparing most normal tissues.

Side Effects

Melphalan can cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Nausea and vomiting: gastrointestinal upset commonly reported during treatment.
  • Myelosuppression: reduced white blood cells, platelets and red cells.
  • Alopecia: hair loss that may be temporary.
  • Fatigue: persistent tiredness affecting daily activities.

Serious or Rare Side Effects

  • Secondary malignancies: risk of developing new cancers after prolonged exposure.
  • Severe infection: due to profound neutropenia.
  • Pulmonary toxicity: interstitial pneumonitis or fibrosis.
  • Renal or cardiac toxicity: impaired kidney function or cardiac complications.

Precautions & Warnings

Melphalan requires careful monitoring and specific safety measures before and during therapy.

  • Blood count monitoring: perform complete blood counts regularly to detect myelosuppression.
  • Renal function assessment: evaluate serum creatinine and adjust dosing if needed.
  • Hepatic function evaluation: check liver enzymes prior to each cycle.
  • Pregnancy risk: avoid use in pregnant women unless benefits outweigh potential fetal harm.
  • Handling precautions: use protective equipment and follow hazardous drug guidelines.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Melphalan may interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Concurrent alkylating agents: additive bone‑marrow toxicity.
  • High‑dose radiation therapy: increased risk of severe tissue damage.
  • Live vaccines: potential for uncontrolled infection due to immunosuppression.
  • Nephrotoxic antibiotics (e.g., aminoglycosides): heightened renal toxicity.
  • Drugs that impair bone‑marrow function (e.g., antimetabolites): profound cytopenias.

Moderate Interactions (Monitor Closely)

  • Azole antifungals: may increase melphalan plasma levels.
  • Allopurinol: can enhance myelosuppressive effects.
  • ACE inhibitors or ARBs: monitor renal parameters.
  • NSAIDs: watch for additive gastrointestinal irritation.
  • Diuretics: assess electrolyte balance and renal function.

Frequently Asked Questions

Melphalan Macure is an intravenous alkylating chemotherapy indicated for adult patients with multiple myeloma, ovarian cancer, melanoma and selected other solid tumours. It is typically used as part of multi‑drug regimens to control disease progression and improve survival outcomes.

Melphalan alkylates DNA bases, forming cross‑links that prevent DNA replication and transcription. This damage triggers cell‑cycle arrest and apoptosis, preferentially affecting rapidly dividing malignant cells while sparing most normal tissues.

The specific dose and schedule of Melphalan Macure are determined by the prescribing oncologist based on the patient’s diagnosis, disease stage, body surface area and renal function. Dosing is individualized and should follow local clinical guidelines.

Melphalan is classified as hazardous to the fetus and is generally contraindicated during pregnancy unless the potential benefit justifies the risk. Breastfeeding is also discouraged because the drug can be excreted in milk and may harm the infant.

To request Melphalan Macure, 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 required import documentation.

Melphalan shares the DNA‑alkylating mechanism of other agents such as cyclophosphamide and busulfan, but it has a distinct pharmacokinetic profile and is often preferred for certain haematologic malignancies like multiple myeloma. Its toxicity spectrum and dosing schedule differ, so clinicians select it based on disease‑specific efficacy and patient tolerance.

Melphalan Macure should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the product in its original packaging until ready for preparation and administration.

Melphalan Macure is supplied as an injectable solution for intravenous infusion. It is administered by a qualified healthcare professional under aseptic conditions, typically over a period of several minutes to an hour, depending on the prescribed protocol.

The most serious risks include severe myelosuppression leading to infection or bleeding, secondary malignancies, pulmonary toxicity, and renal or cardiac complications. Patients should be closely monitored for signs of infection, organ dysfunction and unexpected laboratory abnormalities.

Melphalan Macure is contraindicated in patients with known hypersensitivity to melphalan or any component of the formulation, in those with severe bone‑marrow failure, uncontrolled infections, or in pregnant women unless the therapeutic benefit outweighs the fetal risk.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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