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 formulation for systemic use. It is indicated for the treatment of relapsed or refractory multiple myeloma in patients who have received prior therapies.

GNH India supplies Imnovid as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide.

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 with disease that has progressed after prior treatments.

  • Relapsed/refractory multiple myeloma: Provides a therapeutic option after failure of lenalidomide and bortezomib.
  • Multiple myeloma after prior therapies: Improves disease control when combined with dexamethasone.
  • Multiple myeloma in combination regimens: Enhances anti‑myeloma activity as part of multi‑drug protocols.

How It Works

  • Pomalidomide binds to the cereblon component of the CRL4 E3 ubiquitin ligase complex, directing the degradation of transcription factors Ikaros and Aiolos. This leads to anti‑angiogenic, immunomodulatory, and pro‑apoptotic effects, while also inhibiting TNF‑α production and modulating cytokine release, collectively contributing to its antineoplastic activity.

Side Effects

Adverse reactions to pomalidomide may vary in frequency and severity.

Common Side Effects

  • Neutropenia: reduced neutrophil count increasing infection risk.
  • Anemia: decreased red blood cell levels causing fatigue.
  • Fatigue: general feeling of tiredness.
  • Constipation: difficulty passing stools.
  • Diarrhoea: loose, frequent stools.
  • Rash: skin irritation or redness.

Serious or Rare Side Effects

  • Thromboembolic events: blood clots in veins or arteries.
  • Severe infections: opportunistic or bacterial infections requiring hospitalization.
  • Stevens‑Johnson syndrome: severe skin reaction.
  • Tumour lysis syndrome: rapid tumour cell breakdown.
  • Second primary malignancies: emergence of new cancers.

Precautions & Warnings

When prescribing pomalidomide, clinicians should observe several safety measures.

  • Monitor blood counts: perform regular CBC to detect neutropenia or anemia.
  • Assess thromboembolic risk: evaluate patient history and consider prophylactic anticoagulation.
  • Avoid pregnancy: enforce strict contraception for both patient and partner.
  • Use caution in renal impairment: adjust therapy based on renal function.
  • Store at room temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Pomalidomide may interact with other medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin): may lower pomalidomide plasma levels.
  • Anticoagulants (e.g., warfarin): increased risk of bleeding.
  • Thalidomide or other IMiDs: additive teratogenic risk.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., ketoconazole): may raise pomalidomide exposure.
  • CYP1A2 inhibitors (e.g., fluvoxamine): potential increase in drug levels.
  • NSAIDs: may exacerbate neutropenia or gastrointestinal side effects.

Frequently Asked Questions

Imnovid contains pomalidomide and is used to treat relapsed or refractory multiple myeloma, particularly in patients whose disease has progressed after prior therapies such as lenalidomide and bortezomib.

Pomalidomide binds to cereblon, a component of the CRL4 E3 ubiquitin ligase complex, leading to the targeted degradation of transcription factors Ikaros and Aiolos. This triggers anti‑angiogenic, immunomodulatory, and pro‑apoptotic pathways that help control malignant plasma cells.

The dosage of Imnovid is individualized; the prescribing clinician determines the appropriate dose and schedule based on the patient’s clinical condition, prior treatments, and laboratory parameters.

Pomalidomide is classified as a teratogenic agent. It should not be used during pregnancy, and effective contraception is required for both male and female patients. Safety during breastfeeding has not been established, and nursing is generally discouraged.

To request Imnovid, 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, and any necessary import documentation.

Imnovid (pomalidomide) belongs to the IMiD class, offering a distinct mechanism of action compared with proteasome inhibitors or monoclonal antibodies. It is often used after lenalidomide and bortezomib have failed, providing an

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GNH India Pharmaceuticals Limited

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Last updated:

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