GNH USA

Europe — EMA

Melphalan Tillomed

GNH USA supplies Melphalan Tillomed (Melphalan), an alkylating antineoplastic for multiple myeloma, ovarian cancer and melanoma. Request a quote for supply.

Melphalan

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What is Melphalan?

Melphalan, the active ingredient in Melphalan Tillomed, is an alkylating agent presented as a sterile injectable solution for intravenous use. It treats multiple myeloma, ovarian cancer, malignant melanoma and other solid tumors in adult patients.

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

What is Melphalan used for?

Melphalan is used in chemotherapy regimens targeting malignant cells of specific tumor types.

- Multiple myeloma: reduces malignant plasma‑cell proliferation and improves survival. - Ovarian cancer: incorporated into combination protocols to control tumor growth. - Malignant melanoma: administered in advanced‑disease regimens to achieve tumor regression. - Other solid tumors: added to treatment plans for various solid malignancies to enhance cytotoxic effect.

What are the side effects of Melphalan?

Melphalan may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects: - Nausea and vomiting: gastrointestinal upset frequently reported. - Fatigue: persistent tiredness during treatment. - Myelosuppression: decreased blood cell counts leading to anemia, neutropenia, or thrombocytopenia. - Alopecia: hair loss affecting scalp and body hair.

Serious or Rare Side Effects: - Secondary malignancies: risk of developing new cancers. - Severe infection: due to profound neutropenia. - Pulmonary toxicity: interstitial pneumonitis or fibrosis. - Renal impairment: reduced kidney function.

What precautions apply to Melphalan?

When using Melphalan, clinicians should observe several safety measures to minimize risks.

- Monitor blood counts: perform regular CBC to detect myelosuppression. - Assess organ function: evaluate hepatic and renal function before each cycle. - Avoid in active infection: postpone treatment if severe infection is present. - Use antiemetics: prophylactic medication reduces nausea and vomiting. - Pregnancy and lactation: contraindicated unless benefits outweigh risks; discuss with specialist. - Store at ambient temperature: keep below 25 °C, in original container, protect from moisture and light.

What does Melphalan interact with?

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

Major Interactions (Avoid): - CYP450 inducers: drugs such as rifampin may reduce melphalan exposure. - Live vaccines: concurrent use can increase risk of infection.

Moderate Interactions (Monitor Closely): - Anticoagulants: enhanced bleeding risk; monitor INR/PT. - Nephrotoxic agents: concurrent use may worsen renal impairment. - Other myelosuppressive chemotherapy: additive bone‑marrow suppression; adjust dosing. - Allopurinol: may increase melphalan plasma levels; monitor toxicity.

Frequently asked questions

What is Melphalan Tillomed used for?+
Melphalan Tillomed is an intravenous chemotherapy product used to treat adult patients with multiple myeloma, ovarian cancer, malignant melanoma and selected other solid tumours. It is administered as part of multi‑drug regimens aimed at controlling tumour growth and extending survival.
How does melphalan work as a chemotherapy agent?+
Melphalan belongs to the nitrogen‑mustard class of alkylating agents. It forms covalent bonds with the N7 position of guanine in DNA, creating cross‑links that block DNA replication and transcription. This damage triggers programmed cell death, preferentially affecting rapidly dividing cancer cells.
What is the usual dose of melphalan?+
The specific dose of melphalan is determined by the prescribing oncologist based on the patient’s diagnosis, disease stage, body surface area, renal function and prior therapies. Dosing regimens vary widely, so the prescriber sets the exact amount and schedule for each individual.
Is melphalan safe during pregnancy or breastfeeding?+
Melphalan is classified as contraindicated in pregnancy and breastfeeding because it can cross the placenta and is excreted in breast milk, posing a risk of fetal or infant toxicity. Use is only considered when the potential benefit to the mother outweighs the potential risk to the child, and only under specialist supervision.
How do I order Melphalan Tillomed from GNH USA?+
To request Melphalan Tillomed, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA 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.
How does melphalan compare with other alkylating agents?+
Melphalan shares the DNA‑alkylating mechanism of other nitrogen‑mustard agents such as cyclophosphamide, but it is more lipophilic, allowing better penetration into certain tumour types like multiple myeloma. Its toxicity profile is similar, with notable myelosuppression, but dosing schedules and approved indications differ across agents.
How should Melphalan Tillomed be stored and handled?+
Melphalan Tillomed should be stored at ambient temperature, below 25 °C, in its original sealed container. Protect the product from moisture, direct sunlight and extreme temperatures. Follow standard aseptic techniques when preparing the intravenous solution, and dispose of any unused material according to local hazardous‑waste regulations.
How is Melphalan Tillomed administered to patients?+
Melphalan Tillomed is given by intravenous infusion under the supervision of a qualified healthcare professional. The infusion rate and duration are set by the treating physician, often over 30 minutes to several hours, depending on the prescribed dose and the patient’s tolerance.
What are the most serious risks associated with melphalan therapy?+
The most serious risks include severe myelosuppression leading to life‑threatening infections, secondary malignancies, pulmonary toxicity such as interstitial pneumonitis, and renal impairment. Patients should be monitored closely for signs of infection, respiratory distress, and changes in kidney function throughout treatment.
Who should not receive melphalan treatment?+
Melphalan is contraindicated in patients with known hypersensitivity to melphalan or other nitrogen‑mustard agents, in those with active uncontrolled infections, and in pregnant or breastfeeding women unless the therapeutic benefit justifies the risk. Caution is also advised for patients with severe hepatic or renal dysfunction.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Melphalan
Route
Intravenous Use
Manufacturer
Tillomed Pharma Gmbh
Origin
EU

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