IMJUDO (tremelimumab) by AstraZeneca is ctla-4-directed antibody interactions [moa]. Approved for ctla-4-directed blocking antibody [epc]. First approved in 2022.
Drug data last refreshed 2d ago
IMJUDO (tremelimumab) is a monoclonal antibody that blocks CTLA-4, an immune checkpoint, to enhance T-cell activation and anti-tumor immunity. It is approved for treatment across 25+ solid tumor indications including hepatocellular carcinoma, non-small cell lung cancer, urothelial cancer, pancreatic cancer, and melanoma. The drug works by removing immune suppression, enabling the body's immune system to recognize and attack cancer cells.
Early-stage peak lifecycle with modest Medicare uptake ($2M, 65 claims in 2023) suggests significant growth runway and active brand-building opportunities.
CTLA-4-directed Antibody Interactions
CTLA-4-directed Blocking Antibody
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
A Phase II Study of Single Tremelimumab With Regular Interval Durvalumab Plus Gemcitabine and Cisplatin in Locally Advanced Unresectable/Metastatic Combined Hepatocellular-cholangiocarcinoma
MONTEROSA - Italian Multicenter Observational Study to Evaluate Time to Clinical Hepatic Decompensation, Quality of Life, Effectiveness, and Safety of Tremelimumab Plus Durvalumab in Patients With Advanced or Unresectable Hepatocellular Carcinoma Who Have Received no Prior Systemic Treatment.
Evaluation of RBS2418 in Combination With Tremelimumab Plus Durvalumab in Participants With Advanced Unresectable Hepatocellular Carcinoma
Y-90 Radioembolization, Durvalumab, Tremelimumab, and Zanzalintinib for the Treatment of Unresectable and Locally-Advanced Hepatocellular Carcinoma
Durvalumab and Tremelimumab With or Without Hepatic Arterial Infusion of Chemotherapy in Hepatocellular Carcinoma
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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/moIMJUDO currently shows minimal visible job market presence (0 linked roles) despite peak lifecycle status, suggesting either recent launch-phase staffing completion or lower commercial priority within AstraZeneca's oncology portfolio. Growth opportunities will depend on clinical expansion success and market share gains in competitive solid tumor segments.