Prognia
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🇪🇺EU · EMAAuthorisedATC: L01FX20

Imjudo(tremelimumab)

Carcinoma, Hepatocellular;Carcinoma, Non-Small-Cell Lung

Marketing Authorisation Holder: AstraZeneca AB

EMA Authorisation: 20/02/2023

INN: tremelimumab

Indication

Imjudo in combination with durvalumab is indicated for the first line treatment of adults with advanced or unresectable hepatocellular carcinoma (HCC). Imjudo in combination with durvalumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic non-small cell lung cancer (NSCLC) with no sensitising EGFR mutations or ALK positive mutations.

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.