IMFINZI (durvalumab) by AstraZeneca is programmed death ligand-1 antagonists [moa]. First approved in 2017.
Drug data last refreshed 17h ago · AI intelligence enriched 1mo ago
IMFINZI (durvalumab) is a monoclonal antibody that blocks Programmed Death Ligand-1 (PD-L1), unleashing the immune system to attack cancer cells. It is administered intravenously and is approved for multiple cancer indications including unresectable Stage III non-small cell lung cancer (NSCLC) and other solid tumors. The drug represents a key checkpoint inhibitor in the immuno-oncology landscape.
Product is at peak lifecycle stage with moderate Part D claims; commercial teams are likely focused on market penetration and indication expansion rather than launch activities.
Programmed Death Ligand-1 Antagonists
Programmed Death Ligand-1 Blocker
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Adaptive SBRT Plus Chemoimmunotherapy for ES-SCLC
Tarlatamab and Durvalumab vs. Durvalumab Alone for Limited-Stage-Small Cell Lung Cancer
A Clinical Trial of Gocatamig (MK-6070) With Durvalumab in Participants With Small Cell Lung Cancer (MK-6070-004)
Neoadjuvant Intravesical Nadofaragene Firadenovec With Gemcitabine, Cisplatin and Durvalumab for the Treatment of Muscle Invasive Bladder Cancer, TRIFECTA Trial
A Study of Neoadjuvant-adjuvant Durvalumab and FLOT Chemotherapy Followed by Adjuvant Durvalumab in Chinese Patients With Resectable GC/GEJC.
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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Upgrade to Pro — $25/moWorking on IMFINZI offers exposure to high-stakes immuno-oncology commercialization within a mature, peak-stage product at a global pharma company (AstraZeneca). Career growth depends on driving indication expansion, defending market share against competitors, and supporting clinical/regulatory initiatives to extend the product lifecycle.