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

Melphalan Aqvida

Active Ingredient:
Melphalan
Origin:
EU

Melphalan Aqvida (Melphalan)

Melphalan, the active ingredient in Melphalan Aqvida, is an alkylating agent presented as an intravenous solution for infusion use. It is employed in the treatment of certain hematologic malignancies and solid tumors, including multiple myeloma, ovarian cancer and melanoma, under the supervision of oncology specialists. The drug is formulated for intravenous administration and is regulated as a prescription‑only medication in the European market.

GNH India supplies Melphalan Aqvida as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide. Our supply chain adheres to stringent quality standards, enabling reliable delivery to clinical sites across Europe, Asia, Africa and the Americas.

Manufacturer / TM Owner

Aqvida Gmbh

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Indications & Clinical Uses

Melphalan is an alkylating antineoplastic agent used in chemotherapy regimens for several cancer types.

  • Multiple Myeloma: reduces malignant plasma‑cell proliferation, induces remission, and can extend progression‑free survival when used in appropriate dosing protocols.
  • Ovarian Cancer: enhances the cytotoxic effect of platinum‑based regimens, contributing to tumor shrinkage and improved response rates in advanced disease.
  • Melanoma: provides therapeutic benefit in advanced or metastatic melanoma, often as part of combination protocols to increase overall response.

How It Works

  • Melphalan exerts its antineoplastic activity by forming covalent cross‑links between DNA strands. These interstrand bonds impede DNA replication and transcription, leading to cell‑cycle arrest at the G2/M phase and triggering apoptosis in rapidly dividing tumor cells. The alkylating action preferentially affects malignant cells due to their higher proliferation rate, while normal tissues experience dose‑dependent toxicity.

Side Effects

Melphalan may cause a range of adverse reactions, varying from mild to severe, that require monitoring during therapy.

Common Side Effects

  • Nausea and vomiting
  • Fatigue or weakness
  • Alopecia (hair loss)
  • Mucositis (inflammation of the mouth lining)

Serious or Rare Side Effects

  • Myelosuppression leading to severe neutropenia or anemia
  • Renal toxicity manifested as increased serum creatinine
  • Secondary malignancies such as therapy‑related leukemia

Precautions & Warnings

When using Melphalan, clinicians should observe several precautionary measures to minimize toxicity and ensure safe administration.

  • Monitor blood counts: perform regular complete blood count assessments to detect myelosuppression.
  • Assess renal function: evaluate serum creatinine and creatinine clearance before and during treatment.
  • Evaluate hepatic function: check liver enzymes as melphalan is partially metabolized hepatically.
  • Avoid use in patients with known hypersensitivity to alkylating agents.
  • Use effective contraception: both male and female patients should employ reliable birth control during therapy and for a defined period after.
  • Store at controlled room temperature: keep in original container, protect from light and moisture, and do not freeze.

Avoid Interactions

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

Major Interactions (Avoid)

  • Concurrent use with other alkylating agents: may cause excessive bone‑marrow suppression.
  • High‑dose radiation therapy: increases risk of severe tissue damage.
  • Live vaccines: immunosuppression can lead to uncontrolled infection.

Moderate Interactions (Monitor Closely)

  • CYP450 inducers (e.g., rifampin, phenobarbital): may reduce melphalan plasma levels.
  • Nephrotoxic drugs (e.g., cisplatin, aminoglycosides): heighten risk of renal impairment.
  • Anticoagulants (e.g., warfarin): may enhance bleeding tendency due to thrombocytopenia.

Frequently Asked Questions

Melphalan Aqvida is an intravenous formulation of the alkylating agent melphalan. It is used in oncology to treat certain hematologic cancers such as multiple myeloma and solid tumors including ovarian cancer and advanced melanoma, typically as part of combination chemotherapy protocols.

Melphalan works by forming covalent cross‑links between DNA strands, which blocks DNA replication and transcription. This interference halts cell‑cycle progression, especially at the G2/M checkpoint, and induces programmed cell death (apoptosis) in rapidly dividing cancer cells.

The prescribed dose is determined by the treating physician based on the specific indication, the patient’s body surface area, renal function, and the chosen treatment protocol. Dosing regimens vary and are individualized for each patient.

Melphalan is considered teratogenic and is contraindicated in pregnancy because it can cause fetal harm. It is also excreted in breast milk, so breastfeeding is not recommended during treatment and for a period after the last dose, as advised by the prescribing clinician.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide. After submission, the sales team will verify trade or institutional credentials and respond with pricing, availability, shipping details (including cold‑chain if applicable) and any required import documentation.

Melphalan shares the DNA‑cross‑linking mechanism common to alkylating agents such as cyclophosphamide, but it is often preferred for certain hematologic malignancies because of its higher potency in plasma‑cell disorders. Its toxicity profile, especially myelosuppression and renal effects, may differ, requiring specific monitoring compared with other agents.

Melphalan Aqvida should be stored at controlled room temperature, typically below 25 °C. Keep the vial in its original packaging, protect it from light and moisture, and avoid freezing. Follow aseptic techniques when preparing the solution for intravenous infusion.

The product is supplied as an injectable solution for intravenous infusion. It is administered by a qualified healthcare professional, usually over a period of several minutes to an hour, depending on the prescribed protocol and patient tolerance. Infusion rates and pre‑medication for nausea may be adjusted by the treating physician.

The most serious risks include severe myelosuppression leading to neutropenia, anemia or thrombocytopenia, which can increase infection and bleeding risk; renal toxicity that may impair kidney function; and the potential for secondary malignancies such as therapy‑related leukemia. Patients should be closely monitored for these complications.

Melphalan is contraindicated in patients with known hypersensitivity to melphalan or other alkylating agents, in those with severe renal impairment, and in pregnant or breastfeeding women. Caution is also advised for individuals with pre‑existing bone‑marrow suppression or uncontrolled infections.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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