Imjudo

From WikiMD's Food, Medicine & Wellness Encyclopedia

Imjudo (tremelimumab) is a fully human monoclonal antibody that targets the protein CTLA-4 (cytotoxic T-lymphocyte-associated protein 4). CTLA-4 is a molecule found on T-cells, a type of white blood cell that plays a critical role in the immune system's ability to fight infections and cancer. By inhibiting CTLA-4, Imjudo works to enhance the body's immune response against cancer cells. It is used in the treatment of various types of cancer, including melanoma, non-small cell lung cancer (NSCLC), and others, often in combination with other therapies.

Mechanism of Action[edit | edit source]

Imjudo binds to CTLA-4 and blocks its interaction with its ligands, CD80 and CD86. Normally, CTLA-4 acts as an "off switch" for T-cells, helping to regulate the immune system and prevent it from attacking the body's own cells. By blocking CTLA-4, Imjudo removes this inhibitory signal, allowing the immune system to remain active against cancer cells. This process is known as immune checkpoint blockade, which is a form of cancer immunotherapy.

Clinical Uses[edit | edit source]

Imjudo has been approved for use in various clinical settings, often in combination with other drugs. For example, it has been used in combination with durvalumab, another immunotherapy drug that targets PD-L1, for the treatment of certain types of NSCLC. The combination has shown to improve survival rates in some patients with advanced stages of the disease.

Side Effects[edit | edit source]

As with all immunotherapies, Imjudo can cause a range of side effects, which result from the activation of the immune system. Common side effects include fatigue, diarrhea, skin rash, and itching. However, it can also lead to more severe immune-related adverse effects (irAEs), such as colitis, hepatitis, endocrinopathies, and pneumonitis. These irAEs require prompt recognition and management, often involving corticosteroids or other immunosuppressive medications.

Development and Approval[edit | edit source]

Imjudo was developed by AstraZeneca and has received approval from various regulatory bodies, including the Food and Drug Administration (FDA) in the United States and the European Medicines Agency (EMA) in the European Union. Its development and approval were based on clinical trials that demonstrated its efficacy in improving survival and/or delaying disease progression in certain patient populations.

Future Directions[edit | edit source]

Research is ongoing to explore the full potential of Imjudo in cancer treatment, including its use in combination with other therapies and in other types of cancer. Clinical trials are investigating its effectiveness in earlier stages of cancer and in a wider range of cancer types.

See Also[edit | edit source]

References[edit | edit source]



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Contributors: Prab R. Tumpati, MD