Product image of Melfalan Tillomed (Melphalan) supplied by GNH India

Melfalan Tillomed

Active Ingredient:
Melphalan
Origin:
EU

Melfalan Tillomed (Melphalan)

Melphalan, the active ingredient in Melfalan Tillomed, is an alkylating agent presented as an injectable formulation for intra‑arterial and intravenous use. It is employed in the treatment of certain hematologic malignancies and solid tumours, particularly in adult patients undergoing chemotherapy.

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

Manufacturer / TM Owner

Tillomed Pharma Gmbh

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Indications & Clinical Uses

Melphalan is an alkylating antineoplastic agent used to treat cancers that are sensitive to DNA cross‑linking therapy.

  • Multiple myeloma: helps achieve disease control and prolong survival in eligible patients.
  • Ovarian cancer: used as part of combination regimens to reduce tumour burden.
  • Malignant melanoma: applied in selected cases to induce tumour regression when other therapies are unsuitable.

How It Works

  • Melphalan acts as a bifunctional alkylating agent that forms covalent cross‑links between DNA strands. By binding to the N7 position of guanine bases, it interferes with DNA replication and transcription, triggering cell‑cycle arrest at the G2/M phase and ultimately leading to apoptosis of rapidly dividing cancer cells.

Side Effects

Adverse reactions to melphalan vary in frequency and severity.

Common Side Effects

  • Nausea and vomiting: gastrointestinal upset commonly reported during treatment.
  • Bone‑marrow suppression: decreased white blood cells, platelets, and red cells.
  • Alopecia: reversible hair loss affecting scalp and body hair.
  • Fatigue: persistent tiredness not relieved by rest.
  • Mucositis: inflammation of the mouth and gastrointestinal lining.

Serious or Rare Side Effects

  • Secondary malignancies: risk of developing new cancers after prolonged exposure.
  • Severe infection: opportunistic infections due to profound neutropenia.
  • Pulmonary toxicity: interstitial pneumonitis or fibrosis.
  • Renal toxicity: acute kidney injury in susceptible individuals.
  • Hemorrhagic cystitis: bladder irritation and bleeding.
  • Life‑threatening myelosuppression: pancytopenia requiring transfusion support.

Precautions & Warnings

When using melphalan, clinicians should observe several safety measures.

  • Monitor blood counts: perform regular complete blood count tests to detect myelosuppression.
  • Assess renal function: check serum creatinine and adjust dosing in renal impairment.
  • Evaluate hepatic function: liver enzymes should be monitored before and during therapy.
  • Avoid use in patients with known hypersensitivity to melphalan or related compounds.
  • Contraception: both male and female patients should use effective contraception during treatment and for a defined period afterward.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Concurrent myelosuppressive agents (e.g., high‑dose methotrexate): can cause severe bone‑marrow toxicity.
  • Live viral vaccines: increased risk of vaccine‑derived infection due to immunosuppression.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may exacerbate renal toxicity.
  • Warfarin: melphalan can potentiate anticoagulant effects, requiring INR monitoring.
  • Allopurinol: may increase risk of hypersensitivity reactions.
  • ACE inhibitors: potential for additive renal impairment.
  • Anticonvulsants (e.g., phenytoin): may alter melphalan metabolism.

Frequently Asked Questions

Melfalan Tillomed contains melphalan, an alkylating chemotherapy drug indicated for the treatment of multiple myeloma, ovarian cancer and malignant melanoma. It is administered by a healthcare professional as part of a prescribed cancer‑treatment regimen.

Melphalan binds to DNA at specific sites, creating cross‑links that prevent DNA replication and transcription. This disruption halts cell‑cycle progression, especially in rapidly dividing tumor cells, leading to programmed cell death (apoptosis).

The exact dose of Melfalan Tillomed is individualized by the prescribing oncologist based on factors such as cancer type, disease stage, patient weight, renal function and prior treatment history. No standard dose is provided here.

Melphalan is classified as contraindicated in pregnancy because it can cause fetal harm. It is also not recommended while breastfeeding, as it may be excreted in milk and affect the infant. Patients should discuss fertility and lactation plans with their physician.

To request Melfalan Tillomed, 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.

Melphalan shares the DNA‑cross‑linking mechanism of other alkylators such as cyclophosphamide, but it is more lipophilic, allowing better penetration into certain tissues like bone marrow. Its toxicity profile is similar, though melphalan is often preferred for multiple myeloma because of its proven efficacy in that setting.

Melfalan Tillomed should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight and extreme temperatures. Do not freeze. Follow standard aseptic handling procedures for injectable medicines.

Melfalan Tillomed is given by a qualified healthcare professional via intra‑arterial or intravenous infusion. The infusion rate and duration are determined by the treating physician according to the specific treatment protocol and patient tolerance.

The most serious risks include severe bone‑marrow suppression leading to life‑threatening infections or bleeding, secondary malignancies, pulmonary toxicity, renal impairment and hemorrhagic cystitis. Patients should be monitored closely for signs of infection, respiratory distress, renal dysfunction and urinary symptoms.

Melphalan is contraindicated in patients with known hypersensitivity to the drug or any alkylating agents, in pregnant or nursing women, and in individuals with severe uncontrolled infections or significant organ dysfunction that would increase toxicity risk. Decision to treat should be made by an oncologist after thorough assessment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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