GNH USA

Europe — EMA

Melfalan Hikma

GNH USA supplies Melfalan Hikma (Melphalan), an alkylating antineoplastic for multiple myeloma, ovarian cancer and other malignancies. Request a quote.

Melphalan

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What is Melphalan?

Melphalan, the active ingredient in Melfalan Hikma, is an alkylating agent presented as an intravenous solution for intravenous use. It is employed in the treatment of multiple myeloma, ovarian cancer, malignant melanoma and chronic lymphocytic leukemia, primarily in adult patients requiring systemic chemotherapy.

GNH USA supplies Melfalan Hikma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide, providing reliable access to EU‑sourced chemotherapy agents. The company adheres to stringent quality standards and offers comprehensive logistics support for global distribution.

What is Melphalan used for?

Melphalan is an alkylating chemotherapy agent used in the management of several hematologic and solid tumor malignancies. - Multiple myeloma: reduces malignant plasma cells and prolongs survival. - Ovarian cancer: used in combination regimens to achieve tumor reduction. - Malignant melanoma: employed as part of high‑dose therapy for metastatic disease. - Chronic lymphocytic leukemia: contributes to disease control in refractory cases.

What are the side effects of Melphalan?

Melphalan may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects: - Nausea and vomiting: gastrointestinal upset commonly reported. - Fatigue: persistent tiredness during therapy. - Myelosuppression: reduced blood cell counts causing anemia, neutropenia or thrombocytopenia.

Serious or Rare Side Effects: - Secondary malignancies: risk of therapy‑related cancers. - Severe infection: due to profound neutropenia. - Pulmonary toxicity: interstitial pneumonitis or fibrosis.

What precautions apply to Melphalan?

When using melphalan, several precautions should be observed to minimize risks and ensure safe handling. - Monitor blood counts: regular CBC testing to detect myelosuppression. - Assess renal function: evaluate creatinine clearance before and during therapy. - Use anti‑emetics: prophylactic medication to control nausea and vomiting. - Avoid in pregnancy: melphalan is contraindicated in pregnant patients due to fetal toxicity. - Protective handling: healthcare personnel should wear gloves and use closed system transfer devices. - Store at ambient temperature: keep the solution below 25°C, protected from light, and in the original container.

What does Melphalan interact with?

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

Major Interactions (Avoid): - Live vaccines: may cause severe infection due to immunosuppression. - CYP450 inducers: drugs such as rifampin can reduce melphalan plasma levels. - High‑dose radiotherapy: combined use increases risk of severe tissue damage.

Moderate Interactions (Monitor Closely): - Antifungals (azoles): may increase melphalan toxicity. - Allopurinol: can enhance myelosuppression. - NSAIDs: may exacerbate renal toxicity.

Frequently asked questions

What is Melfalan Hikma used for?+
Melfalan Hikma contains melphalan, an alkylating chemotherapy agent indicated for the treatment of multiple myeloma, ovarian cancer, malignant melanoma and chronic lymphocytic leukemia. It is administered intravenously under the supervision of an oncologist as part of a systemic cancer‑treatment regimen.
How does melphalan work?+
Melphalan exerts its antineoplastic activity by forming covalent cross‑links between DNA strands, primarily at the N7 position of guanine bases. These cross‑links prevent DNA replication and transcription, leading to cell‑cycle arrest and apoptosis of rapidly dividing tumor cells.
What is the usual dose of melphalan?+
The dose of melphalan is individualized by the prescribing oncologist based on the specific cancer type, disease stage, patient weight, renal function and treatment protocol. Dosage regimens are determined in a clinical setting and are not standardized across all patients.
Is melphalan safe in pregnancy or breastfeeding?+
Melphalan is classified as pregnancy category D, indicating evidence of fetal risk, and it is contraindicated during pregnancy. It is also excreted in breast milk, so breastfeeding is not recommended while receiving treatment.
How do I order Melfalan Hikma from GNH USA?+
To request Melfalan Hikma, 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 any cold‑chain requirements) and necessary import documentation.
How does melphalan compare with other alkylating agents?+
Compared with other alkylating agents such as cyclophosphamide or busulfan, melphalan has a higher potency and is often used for high‑dose regimens in hematologic malignancies. Its toxicity profile includes pronounced myelosuppression, but it may offer improved response rates in certain cancers like multiple myeloma.
What are the storage and handling requirements for Melfalan Hikma?+
Melfalan Hikma should be stored at controlled room temperature, below 25 °C, protected from light, and kept in its original packaging to maintain stability. The solution must be handled with protective gloves and prepared in a sterile environment to avoid contamination.
How is Melfalan Hikma administered?+
The product is supplied as an intravenous solution that is infused directly into a vein by a qualified healthcare professional. Administration is typically performed in a clinical setting, with infusion rates and pre‑medication (e.g., anti‑emetics) determined by the treating physician.
What are the most serious risks associated with melphalan therapy?+
The most serious risks include severe myelosuppression leading to infection or bleeding, secondary malignancies, pulmonary toxicity such as interstitial pneumonitis, and renal impairment. Patients should be closely monitored for signs of infection, respiratory distress and changes in kidney function throughout treatment.
Who should not receive melphalan?+
Melphalan is contraindicated in pregnant women, patients with known hypersensitivity to melphalan or related compounds, and individuals with severe renal impairment where dose adjustment is not feasible. Caution is also advised for patients with active infections or uncontrolled cardiac disease.
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
Hikma Farmacêutica (Portugal), S.A.
Origin
EU

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