Product image of Imnovid (Pomalidomide) supplied by GNH India

Imnovid

Active Ingredient:
Pomalidomide
Origin:
EU

Imnovid (Pomalidomide)

Pomalidomide, the active ingredient in Imnovid, is an immunomodulatory imide drug (IMiD) presented as an oral tablet for oral use. It is indicated for the treatment of relapsed or refractory multiple myeloma in adult patients who have received prior therapies.

GNH India supplies Imnovid as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide, ensuring quality and regulatory compliance across markets.

Manufacturer / TM Owner

Bristol-Myers Squibb Pharma Eeig

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Indications & Clinical Uses

Imnovid is an immunomodulatory agent used in the management of multiple myeloma, particularly in patients whose disease has progressed after prior therapies.

  • Relapsed multiple myeloma: provides disease control after previous treatment failure.
  • Refractory multiple myeloma: offers a therapeutic option when disease does not respond to earlier regimens.
  • Patients previously treated with lenalidomide and bortezomib: extends progression‑free survival in this heavily pre‑treated population.

How It Works

  • Pomalidomide binds to the cereblon component of the CRL4 E3 ubiquitin ligase complex, altering substrate specificity. This leads to ubiquitination and proteasomal degradation of transcription factors Ikaros and Aiolos, resulting in immunomodulation, anti‑angiogenic effects, and direct anti‑myeloma activity through apoptosis and cell‑cycle arrest.

Side Effects

Adverse reactions to Imnovid may vary in frequency and severity.

Common Side Effects

  • Fatigue: persistent tiredness reported by many patients.
  • Neutropenia: reduced neutrophil count increasing infection risk.
  • Anemia: lowered red blood cell levels causing weakness.
  • Constipation: decreased bowel movements.
  • Diarrhea: loose stools.
  • Rash: mild skin eruptions.

Serious or Rare Side Effects

  • Thromboembolic events: deep vein thrombosis or pulmonary embolism.
  • Severe neutropenia: markedly low neutrophil counts requiring medical intervention.
  • Stevens‑Johnson syndrome: severe skin reaction.
  • Tumor lysis syndrome: rapid tumor cell breakdown.
  • Second primary malignancies: emergence of new cancers.

Precautions & Warnings

Before initiating Imnovid, several safety considerations should be observed.

  • Pregnancy avoidance: contraindicated in pregnancy (Category X).
  • Teratogenic risk: ensure effective contraception for both patient and partner.
  • Blood monitoring: perform regular complete blood counts to detect cytopenias.
  • Infection risk: monitor for signs of infection and manage promptly.
  • Thromboembolism prophylaxis: assess risk factors and consider anticoagulation when appropriate.
  • Store at ambient temperature: keep below 25 °C, protect from moisture and light.

Avoid Interactions

Imnovid may interact with other medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors: may increase pomalidomide exposure.
  • Strong CYP3A4 inducers: may reduce pomalidomide exposure.
  • Anticoagulants: increased risk of bleeding.
  • Live vaccines: contraindicated due to immunosuppression.

Moderate Interactions (Monitor Closely)

  • Antihistamines: may enhance sedation.
  • NSAIDs: may increase risk of thrombocytopenia.
  • CYP3A4 substrates: may require dose adjustment.
  • Hormonal contraceptives: efficacy may be reduced, consider alternative methods.

Frequently Asked Questions

Imnovid is prescribed for adults with relapsed or refractory multiple myeloma, particularly when the disease has progressed after prior therapies such as lenalidomide and bortezomib. It helps control tumor growth and extend progression‑free survival.

Pomalidomide binds to cereblon, a component of the CRL4 E3 ubiquitin ligase complex, causing degradation of transcription factors Ikaros and Aiolos. This triggers immunomodulatory, anti‑angiogenic, and direct anti‑myeloma effects, leading to tumor cell apoptosis and reduced proliferation.

The specific dose and schedule of Imnovid are determined by the prescribing physician based on the patient’s clinical condition, prior treatments, and laboratory parameters. Dosage adjustments may be required for renal or hepatic impairment.

Imnovid is classified as Pregnancy Category X due to its teratogenic potential. It should not be used by pregnant women, and effective contraception is required for both patients and male partners. Breastfeeding is not recommended while on therapy.

To place an order, submit an enquiry on the Imnovid 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 and any necessary import documentation.

Imnovid belongs to the immunomodulatory imide drug class, similar to lenalidomide and thalidomide, but it is more potent and effective in patients who have become refractory to those agents. Compared with proteasome inhibitors, it offers a distinct mechanism focusing on cereblon‑mediated degradation of transcription factors.

Imnovid tablets should be stored at ambient temperature, below 25 °C, in the original packaging to protect from moisture and light. Keep the product out of reach of children and do not use if the packaging is damaged.

Imnovid is taken orally, usually once daily on a schedule prescribed by the treating physician. It is swallowed with water and may be taken with or without food, depending on the prescriber’s instructions.

The most serious risks include severe neutropenia, thromboembolic events such as deep‑vein thrombosis or pulmonary embolism, and rare but severe skin reactions like Stevens‑Johnson syndrome. Patients should be monitored closely for signs of infection, bleeding, or sudden skin changes.

Imnovid should not be used by individuals who are pregnant, have uncontrolled infections, or have a known hypersensitivity to pomalidomide or any component of the formulation. Patients with a high risk of thrombosis should be evaluated carefully before initiation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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