Product image of Imjudo (Tremelimumab) supplied by GNH India

Imjudo

Active Ingredient:
Tremelimumab
Origin:
EU

Imjudo (Tremelimumab)

Tremelimumab, the active ingredient in Imjudo, is a CTLA‑4 inhibitor presented as an intravenous formulation for infusion use. It is employed in oncology to enhance T‑cell mediated immune responses against certain advanced solid tumours. The drug is indicated for patients with unresectable or metastatic disease where standard therapies have limited efficacy.

GNH India supplies Imjudo as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres, hospitals and specialty pharmacies worldwide. The company adheres to stringent quality standards and provides cold‑chain logistics for biologic products.

Manufacturer / TM Owner

Astrazeneca Ab

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Indications & Clinical Uses

Imjudo is a CTLA‑4 checkpoint inhibitor used in the treatment of specific solid tumours and in clinical investigation of other cancers.

  • Malignant mesothelioma: improves overall survival when combined with durvalumab in patients with unresectable disease.
  • Advanced non‑small cell lung cancer (investigational): being evaluated for efficacy in combination regimens.
  • Metastatic melanoma (investigational): studied as part of checkpoint‑inhibitor combination therapies.

How It Works

  • Tremelimumab is a monoclonal antibody that binds to the cytotoxic T‑lymphocyte‑associated protein 4 (CTLA‑4) receptor on T cells, blocking its interaction with the co‑stimulatory molecules CD80/CD86. This inhibition releases the brake on T‑cell activation, enhancing proliferation and cytokine release, thereby strengthening the antitumor immune response.

Side Effects

Common Side Effects

  • Fatigue: mild to moderate tiredness experienced during treatment.
  • Rash: skin erythema or maculopapular eruptions.
  • Diarrhea: loose stools, sometimes watery.
  • Nausea: feeling of sickness, occasional vomiting.
  • Infusion‑related reactions: flushing, chills, or mild hypotension during administration.
  • Pruritus: itching of the skin.

Serious or Rare Side Effects

  • Immune‑mediated colitis: severe inflammation of the colon requiring prompt treatment.
  • Hepatitis: liver inflammation with elevated enzymes.
  • Endocrinopathies: thyroiditis, hypophysitis, or adrenal insufficiency.
  • Pneumonitis: inflammation of lung tissue, potentially life‑threatening.
  • Severe infusion reactions: anaphylaxis or cytokine release syndrome.
  • Myocarditis: inflammation of heart muscle, rare but critical.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient history and monitor for immune‑related events.

  • Monitor immune‑related adverse events: perform regular assessments of organ function and symptom review.
  • Assess pre‑existing autoimmune disease: weigh risk versus benefit and consider close monitoring.
  • Screen for infections: test for latent tuberculosis, hepatitis B/C, and HIV before treatment.
  • Avoid concurrent high‑dose immunosuppressants unless medically required: they may diminish therapeutic effect.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Tremelimumab may interact with other agents that modify immune function.

Major Interactions (Avoid)

  • Concurrent use with other immune checkpoint inhibitors: heightened risk of severe immune toxicity.
  • Live vaccines: contraindicated due to potential for uncontrolled infection.
  • High‑dose systemic steroids or other strong immunosuppressants: may reduce antitumor efficacy.

Moderate Interactions (Monitor Closely)

  • CYP450 substrate drugs: monitor levels as immune modulation can affect metabolism.
  • Anticoagulants: observe for bleeding if severe infusion reactions cause thrombocytopenia.
  • Non‑live vaccines: efficacy may be reduced; assess immune response.

Frequently Asked Questions

Imjudo (tremelimumab) is a CTLA‑4 checkpoint inhibitor used primarily for the treatment of unresectable malignant mesothelioma, often in combination with durvalumab. It is also being evaluated in clinical studies for other advanced solid tumours such as non‑small cell lung cancer and melanoma.

Tremelimumab binds to the CTLA‑4 receptor on T cells, preventing its interaction with CD80/CD86 on antigen‑presenting cells. This blockade releases the inhibitory signal, leading to enhanced T‑cell activation, proliferation, and a stronger immune response against tumour cells.

The dosing regimen for Imjudo is determined by the prescribing oncologist based on the specific indication, patient characteristics, and treatment protocol. Healthcare professionals set the dose and schedule according to approved guidelines and clinical judgment.

Safety data for tremelimumab in pregnancy or lactation are limited. It is generally advised to avoid use during pregnancy unless the potential benefit justifies the risk, and breastfeeding is not recommended because the drug may be excreted in milk.

To request Imjudo, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed), and import documentation.

Imjudo targets CTLA‑4, whereas many alternatives such as pembrolizumab or nivolumab target the PD‑1/PD‑L1 pathway. CTLA‑4 blockade can produce broader T‑cell activation but may be associated with a higher incidence of immune‑related adverse events compared with PD‑1 inhibitors.

Imjudo must be stored refrigerated at 2‑8 °C. It should be kept in its original packaging, protected from light, and must not be frozen or shaken. Proper cold‑chain logistics are essential to maintain product stability.

Imjudo is given as an intravenous infusion under the supervision of qualified healthcare professionals. The infusion rate and duration are determined by the treating physician and follow the recommended administration protocol for the specific indication.

The most serious risks include immune‑mediated colitis, hepatitis, pneumonitis, endocrinopathies (such as thyroiditis or hypophysitis), myocarditis, and severe infusion reactions. Prompt recognition and management of these events are critical to patient safety.

Imjudo is contraindicated in patients with active, uncontrolled autoimmune diseases, those receiving live vaccines, or individuals with known hypersensitivity to tremelimumab or any of its excipients. Caution is also advised for patients with a history of severe immune‑related adverse events.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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