Product image of Melfal뿯½n Zentiva (Melphalan Hydrochloride) supplied by GNH India

Melfal뿯½n Zentiva

Active Ingredient:
Melphalan Hydrochloride
Origin:
EU

Melfal뿯½n Zentiva (Melphalan Hydrochloride)

Melphalan Hydrochloride, the active ingredient in Melfal뿯½n Zentiva, is an alkylating agent presented as an intravenous formulation for use in cancer chemotherapy. It is employed to treat various hematologic and solid tumors in adult patients.

GNH India supplies Melfal뿯½n Zentiva as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide, adhering to stringent quality standards and providing regulatory‑compliant distribution across global markets, ensuring product integrity from manufacturing to delivery.

Manufacturer / TM Owner

Zentiva, K.S.

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Indications & Clinical Uses

Melphalan Hydrochloride is used in chemotherapy regimens targeting specific malignancies.

  • Multiple myeloma: reduces malignant plasma‑cell proliferation and improves survival outcomes.
  • Ovarian cancer: enhances cytotoxic effect when combined with platinum‑based agents.
  • Melanoma: provides alkylating activity for refractory metastatic disease.
  • Chronic lymphocytic leukemia: induces DNA cross‑linking to limit leukemic cell growth.

How It Works

  • Melphalan Hydrochloride exerts its antineoplastic activity by forming covalent bonds with the N7 position of guanine bases in DNA. This alkylation creates intra‑ and interstrand cross‑links that impede DNA replication and transcription, ultimately triggering apoptosis in rapidly dividing tumor cells. The nitrogen‑mustard moiety enables these irreversible DNA modifications, making it effective against both hematologic and solid tumors.

Side Effects

Administration of melphalan may be associated with a range of adverse reactions, varying in frequency and severity.

Common Side Effects

  • Nausea and vomiting.
  • Fatigue and general weakness.
  • Myelosuppression manifested as neutropenia, anemia or thrombocytopenia.
  • Mucositis or oral ulceration.
  • Alopecia (hair loss).

Serious or Rare Side Effects

  • Secondary malignancies such as therapy‑related leukemia.
  • Severe infections due to profound neutropenia.
  • Pulmonary toxicity, including interstitial pneumonitis.
  • Renal impairment or acute kidney injury.
  • Hepatotoxicity with elevated liver enzymes.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate baseline organ function and monitor patients closely throughout treatment.

  • Blood Count Monitoring: Perform complete blood counts regularly to detect myelosuppression.
  • Renal Function Assessment: Check serum creatinine and adjust dosing if renal impairment is present.
  • Hepatic Function Assessment: Evaluate liver enzymes and bilirubin before and during therapy.
  • Hypersensitivity Awareness: Discontinue if signs of allergic reaction such as rash, pruritus or anaphylaxis occur.
  • Protective Handling: Use appropriate personal protective equipment to avoid occupational exposure.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Melphalan may interact with other medicines, altering efficacy or increasing toxicity.

Major Interactions (Avoid)

  • Concurrent use with other alkylating agents (e.g., cyclophosphamide) due to cumulative bone‑marrow toxicity.
  • Co‑administration with nephrotoxic drugs (e.g., cisplatin) can exacerbate renal injury.
  • Live vaccines should be avoided because of immunosuppression.

Moderate Interactions (Monitor Closely)

  • Anticoagulants (e.g., warfarin) may increase bleeding risk; monitor coagulation parameters.
  • Allopurinol can potentiate melphalan toxicity; adjust dose or monitor closely.
  • CYP450 inducers or inhibitors may affect melphalan metabolism; observe for altered blood counts.

Frequently Asked Questions

Melfal뿯½n Zentiva contains melphalan hydrochloride, an alkylating chemotherapy agent indicated for the treatment of multiple myeloma, ovarian cancer, melanoma and chronic lymphocytic leukemia in adult patients.

Melphalan alkylates the N7 position of guanine residues in DNA, creating intra‑ and interstrand cross‑links that block DNA replication and transcription, ultimately leading to apoptosis of rapidly dividing cancer cells.

The dose of melphalan is individualized by the treating physician based on the specific cancer type, disease stage, patient weight, renal function and prior therapy. No fixed regimen is provided here.

Melphalan is classified as contraindicated in pregnancy because of its potential to cause fetal harm. It is also not recommended while breastfeeding, as it can be excreted in milk and affect the infant.

Submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies 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‑cross‑linking mechanism of other nitrogen‑mustard agents such as cyclophosphamide, but it is often preferred for certain hematologic malignancies and for high‑dose regimens prior to stem‑cell transplantation because of its potency and pharmacokinetic profile.

The product should be stored at 2‑8 °C, protected from light, and kept in its original container. Do not freeze or shake the vial. Follow standard aseptic techniques when preparing the intravenous solution.

Melfal뿯½n Zentiva is given by intravenous infusion under the supervision of a qualified healthcare professional. The infusion rate and dilution are determined by the prescriber and institutional protocols.

Serious risks include severe myelosuppression leading to infection or bleeding, secondary malignancies such as therapy‑related leukemia, pulmonary toxicity, and renal or hepatic impairment. Patients should be monitored closely for these events.

Melphalan is contraindicated in patients with known hypersensitivity to the drug, those with severe bone‑marrow failure, uncontrolled infections, or significant renal or hepatic dysfunction that cannot be corrected. Caution is also advised in pregnant or nursing women.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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