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 16h ago · AI intelligence enriched 1mo ago
IMJUDO (tremelimumab) is a CTLA-4-directed blocking monoclonal antibody approved in October 2022 for cancer immunotherapy. It works by releasing immune checkpoints to enhance T-cell activation and anti-tumor immunity. The drug is administered intravenously as an injectable solution.
Product is in peak lifecycle stage with modest early uptake (65 Part D claims in 2023), indicating a growing but still-developing commercial franchise with potential for team expansion.
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
Worked on IMJUDO at AstraZeneca? Share your interview experience or compensation data (+7 days Pro)
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.
Upgrade to Pro to access Medicare Part D spending data and other premium pharma intelligence.
Upgrade to Pro — $25/moUpgrade to Pro to access CMS Part B ASP pricing data and other premium pharma intelligence.
Upgrade to Pro — $25/moWorking on IMJUDO offers exposure to specialty oncology commercialization in a competitive, high-stakes CTLA-4 inhibitor market dominated by an entrenched competitor. The role emphasizes regulatory compliance, physician engagement around immune-mediated toxicities, and differentiation strategies in a nascent product lifecycle with moderate growth potential.