GNH USA

Europe — EMA

Imfinzi

GNH USA supplies Imfinzi (Durvalumab), a PD‑L1 inhibitor for extensive‑stage small cell lung cancer, unresectable stage III NSCLC and advanced urothelial

Durvalumab

Request sourcing

1
Pack/s

What is Durvalumab?

Durvalumab, the active ingredient in Imfinzi, is a monoclonal antibody presented as a 500 mg powder for solution for injection for intravenous use. It treats certain advanced cancers, including extensive‑stage small cell lung cancer, unresectable stage III non‑small cell lung cancer after chemoradiation, and selected urothelial, biliary tract and metastatic cancers. It is also indicated for locally advanced or metastatic urothelial carcinoma after platinum‑based chemotherapy, and for biliary tract cancer in combination with chemotherapy. GNH USA supplies Imfinzi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide, with established cold‑chain logistics and regulatory support.

What is Durvalumab used for?

Imfinzi (durvalumab) is a PD‑L1 inhibitor used in several advanced solid‑tumor indications. - Extensive‑stage small cell lung cancer (ES‑SCLC): improves overall survival when given as maintenance therapy after first‑line chemotherapy. - Unresectable stage III non‑small cell lung cancer (NSCLC) after chemoradiation: serves as consolidation therapy to reduce recurrence. - Locally advanced or metastatic urothelial carcinoma after platinum‑based chemotherapy: provides an additional line of treatment to extend disease control. - Biliary tract cancer in combination with chemotherapy: used to enhance response rates in patients with advanced disease.

What are the side effects of Durvalumab?

Imfinzi may be associated with a range of adverse reactions observed in clinical use.

Common Side Effects: - Fatigue: persistent tiredness reported by patients. - Nausea: mild to moderate nausea. - Decreased appetite: reduced food intake. - Skin rash: mild dermatologic reactions.

Serious or Rare Side Effects: - Immune‑mediated pneumonitis: inflammation of lung tissue that can be severe. - Hepatitis: liver inflammation with elevated enzymes. - Endocrine disorders: thyroiditis or adrenal insufficiency requiring hormone replacement.

What precautions apply to Durvalumab?

Before initiating Imfinzi, clinicians should consider several safety measures. - Monitor for immune‑related adverse events: assess organ function regularly. - Evaluate for pre‑existing autoimmune disease: consider risk‑benefit before initiating. - Conduct baseline and periodic imaging: detect pneumonitis early. - Counsel patients on infection signs: report fever or cough promptly. - Store at 2‑8 °C: keep refrigerated, protect from light, do not freeze or shake.

What does Durvalumab interact with?

Imfinzi can interact with other therapies that affect the immune system or organ function.

Major Interactions (Avoid): - Live vaccines: concurrent administration may reduce vaccine efficacy and increase risk. - High‑dose corticosteroids: may diminish therapeutic effect. - Organ transplant immunosuppression: increased risk of graft rejection.

Moderate Interactions (Monitor Closely): - Combination chemotherapy: monitor for overlapping toxicities. - Other PD‑1/PD‑L1 inhibitors: avoid sequential use without appropriate washout period.

Frequently asked questions

What conditions is Imfinzi used to treat?+
Imfinzi (durvalumab) is approved for several advanced solid‑tumor indications, including extensive‑stage small cell lung cancer, unresectable stage III non‑small cell lung cancer after chemoradiation, locally advanced or metastatic urothelial carcinoma following platinum‑based chemotherapy, and biliary tract cancer when given together with chemotherapy.
How does durvalumab work?+
Durvalumab is a monoclonal antibody that binds to the programmed death‑ligand 1 (PD‑L1) protein on tumor and immune cells. By blocking PD‑L1 from engaging its receptors PD‑1 and CD80, the drug lifts the inhibitory signal on T‑cells, restoring their ability to recognize and attack cancer cells.
What is the usual dose of Imfinzi?+
The specific dose and schedule of Imfinzi are determined by the treating physician based on the approved indication, patient weight, and clinical condition. In practice, the product is supplied as a 500 mg vial that is reconstituted and administered intravenously according to the prescriber’s instructions.
Is Imfinzi safe during pregnancy or breastfeeding?+
Safety data for durvalumab in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision should be made in consultation with a healthcare professional.
How do I order Imfinzi from GNH USA?+
To request Imfinzi, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide, and will ask for trade or institutional credentials. The sales team then provides pricing, availability, shipping details—including cold‑chain handling where required—and assists with any necessary import documentation.
How does Imfinzi compare with other PD‑L1 inhibitors?+
Imfinzi (durvalumab) shares the same target as other PD‑L1 inhibitors such as atezolizumab and avelumab, but differences exist in dosing intervals, approved indications, and clinical trial outcomes. For example, durvalumab is uniquely approved as consolidation therapy after chemoradiation for stage III NSCLC, whereas atezolizumab has separate approvals for metastatic bladder cancer and first‑line NSCLC.
How should Imfinzi be stored and handled?+
Imfinzi must be stored in a refrigerator at 2‑8 °C (36‑46 °F). Keep the vial in its original packaging, protect it from light, and do not freeze or shake. Once reconstituted, the solution should be used within the time frame specified in the product labeling and maintained under the same temperature conditions.
How is Imfinzi administered?+
The powder is reconstituted with the supplied diluent to create a sterile solution for intravenous infusion. The prepared solution is administered by a healthcare professional, typically over 60 minutes, through an IV line. Administration settings follow standard aseptic techniques and monitoring for infusion‑related reactions.
What are the most serious risks to watch for with Imfinzi?+
The most serious immune‑mediated adverse events include pneumonitis (inflammation of lung tissue), hepatitis (liver inflammation), and endocrine disorders such as thyroiditis or adrenal insufficiency. These conditions can be severe or life‑threatening and require prompt medical evaluation, monitoring, and appropriate management, often including corticosteroid therapy.
Who should not use Imfinzi?+
Imfinzi is contraindicated in patients with known hypersensitivity to durvalumab or any of its excipients. Caution is advised for individuals with active autoimmune diseases, organ transplants, or those receiving systemic immunosuppressants, as the drug may exacerbate underlying conditions or increase the risk of graft rejection.
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
Durvalumab
Route
Intravenous Use
Manufacturer
Astrazeneca Ab
Origin
EU

Related products