Product image of Lenalidomide Glenmark (Lenalidomide) supplied by GNH India

Lenalidomide Glenmark

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomide Glenmark (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomide Glenmark, is an immunomodulatory agent presented as an oral tablet for oral use. It treats multiple myeloma, myelodysplastic syndromes, and mantle cell lymphoma in adult patients.

GNH India supplies Lenalidomide Glenmark as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Glenmark Arzneimittel Gmbh

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Indications & Clinical Uses

  • Lenalidomide is an immunomodulatory agent used in hematologic malignancies.
  • Multiple Myeloma: improves disease control and prolongs progression‑free survival in relapsed or refractory patients.
  • Myelodysplastic Syndromes: reduces transfusion dependence and improves blood counts in patients with del(5q) cytogenetic abnormality.
  • Mantle Cell Lymphoma: contributes to disease control in relapsed or refractory mantle cell lymphoma.

How It Works

  • Lenalidomide binds to the cereblon component of the CRL4 E3 ubiquitin ligase complex, promoting ubiquitination and proteasomal degradation of transcription factors Ikaros and Aiolos. This leads to modulation of cytokine production, inhibition of angiogenesis, and anti‑proliferative effects on malignant plasma cells and other hematologic cancer cells.

Side Effects

Common Side Effects

  • Fatigue or weakness.
  • Nausea, vomiting or loss of appetite.
  • Diarrhoea or constipation.
  • Rash or mild skin irritation.
  • Decreased neutrophil count (neutropenia).
  • Low platelet count (thrombocytopenia).

Serious or Rare Side Effects

  • Thromboembolic events such as deep‑vein thrombosis or pulmonary embolism.
  • Severe neutropenia or infections requiring hospitalization.
  • Secondary primary malignancies.
  • Hepatotoxicity with elevated liver enzymes.
  • Severe skin reactions including Stevens‑Johnson syndrome.
  • Cardiac arrhythmias or heart failure exacerbation.

Precautions & Warnings

  • Lenalidomide requires careful monitoring and specific safety measures.
  • Pregnancy: contraindicated (Category X); avoid use in pregnant women and ensure effective contraception.
  • Thromboembolism risk: assess patient history and consider prophylactic anticoagulation.
  • Hematologic monitoring: perform regular complete blood counts to detect neutropenia or anemia.
  • Renal impairment: use with caution and monitor renal function closely.
  • Drug interactions: review concomitant medications for potential CYP or immunosuppressive effects.
  • Store at ambient temperature: keep below 25°C, protect from moisture and light in the original packaging.

Avoid Interactions

Lenalidomide may interact with several drug classes; monitoring is essential.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers: may reduce lenalidomide exposure.
  • Anticoagulants: increased risk of thrombosis when combined without prophylaxis.
  • Live vaccines: heightened risk of severe infection.

Moderate Interactions (Monitor Closely)

  • Immunosuppressants: may enhance overall immunosuppression.
  • Nephrotoxic agents: monitor renal function closely.
  • Hormonal contraceptives: reduced efficacy; advise alternative contraception methods.

Frequently Asked Questions

Lenalidomide Glenmark is prescribed for adult patients with multiple myeloma, myelodysplastic syndromes that have a del(5q) chromosomal abnormality, and mantle cell lymphoma, particularly in relapsed or refractory disease settings.

Lenalidomide binds to cereblon, a component of the CRL4 E3 ubiquitin ligase complex, leading to the degradation of transcription factors Ikaros and Aiolos. This action modulates immune responses, inhibits new blood‑vessel formation, and reduces proliferation of malignant cells.

The specific dose and schedule of Lenalidomide Glenmark are determined by the prescribing physician based on the patient’s diagnosis, disease stage, renal function, and other clinical factors. Patients should follow the prescriber’s instructions exactly.

Lenalidomide is classified as Pregnancy Category X, meaning it is contraindicated in pregnancy due to a high risk of fetal harm. It is also not recommended for breastfeeding mothers because it may be excreted in breast milk.

To place an order, 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.

Lenalidomide belongs to the immunomodulatory drug class, offering a distinct mechanism compared with proteasome inhibitors or monoclonal antibodies. It is often used in combination regimens and may provide benefits in patients who have progressed after other standard therapies.

Store Lenalidomide Glenmark at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture and direct light, and avoid storing it in humid environments.

Lenalidomide Glenmark is taken orally, usually as a tablet, with or without food as directed by the prescriber. Swallow the tablet whole with a glass of water and follow the dosing schedule provided by the healthcare professional.

Serious risks include thromboembolic events such as deep‑vein thrombosis, severe neutropenia leading to infection, secondary primary malignancies, and significant liver toxicity. Patients should be monitored regularly for these complications.

Lenalidomide Glenmark should not be used by pregnant women, individuals with uncontrolled infections, or patients with severe renal impairment without appropriate monitoring. It is also contraindicated in patients with known hypersensitivity to lenalidomide or any of its excipients.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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