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

Lenalidomide Biocon

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomide Biocon (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomide Biocon, is an immunomodulatory agent presented as an oral tablet for oral use. It is indicated for the treatment of multiple myeloma, myelodysplastic syndromes and mantle cell lymphoma in adult patients, typically within combination therapy regimens. The drug is administered orally and absorbed systemically.

GNH India supplies Lenalidomide Biocon as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, and pharmacies worldwide. The product complies with EU market standards and is manufactured under strict quality controls.

Manufacturer / TM Owner

Biocon Pharma Malta I Limited

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Indications & Clinical Uses

Lenalidomide is used in hematologic malignancies and related disorders, targeting abnormal plasma cells and dysplastic bone marrow.

  • Multiple Myeloma: reduces disease progression and improves survival when used in combination regimens.
  • Myelodysplastic Syndromes: decreases transfusion dependence and modifies disease course in patients with del(5q) cytogenetic abnormality.
  • Mantle Cell Lymphoma: contributes to tumor control as part of salvage therapy in relapsed or refractory cases.

How It Works

  • Lenalidomide binds to the cereblon component of the CRL4‑E3 ubiquitin ligase complex, altering its substrate specificity. This leads to ubiquitination and proteasomal degradation of transcription factors Ikaros (IKZF1) and Aiolos (IKZF3), resulting in anti‑angiogenic effects, modulation of cytokine production, and enhanced immune‑mediated tumor cell killing. The downstream effects include reduced proliferation of malignant plasma cells and restoration of normal immune surveillance, while also decreasing vascular endothelial growth factor levels in the tumor microenvironment.

Side Effects

Lenalidomide may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Fatigue: persistent tiredness or lack of energy.
  • Diarrhea: loose stools, often mild to moderate.
  • Nausea: feeling of sickness, may be accompanied by vomiting.
  • Rash: skin redness or mild eruption.
  • Low blood counts: decreased neutrophils, platelets, or red cells.
  • Peripheral neuropathy: tingling or numbness in extremities.

Serious or Rare Side Effects

  • Thromboembolic events: deep vein thrombosis or pulmonary embolism.
  • Severe neutropenia: markedly low neutrophil count increasing infection risk.
  • Severe thrombocytopenia: very low platelet count leading to bleeding.
  • Secondary primary malignancies: emergence of new cancers.
  • Hepatotoxicity: significant liver enzyme elevation or liver injury.

Precautions & Warnings

When prescribing lenalidomide, clinicians should consider several safety and handling precautions.

  • Monitor blood counts: perform regular CBC to detect cytopenias.
  • Assess thrombotic risk: evaluate history of clotting disorders and consider prophylaxis.
  • Evaluate renal function: adjust use in patients with impaired kidney function.
  • Avoid pregnancy: ensure effective contraception for both male and female patients of reproductive potential.
  • Review drug interactions: check concomitant medications that may increase toxicity.
  • Store at ambient temperature: keep below 25 °C in the original container, protect from moisture and light.

Avoid Interactions

Lenalidomide can interact with other medicines, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers: may reduce lenalidomide exposure.
  • Anticoagulants (e.g., warfarin): increased risk of bleeding when combined with thrombocytopenia.

Moderate Interactions (Monitor Closely)

  • Immunosuppressants (e.g., cyclosporine): may enhance hematologic toxicity.
  • P-glycoprotein inhibitors: potential increase in plasma levels.
  • Live vaccines: risk of infection due to immunomodulation.
  • NSAIDs: may exacerbate gastrointestinal irritation.

Frequently Asked Questions

Lenalidomide Biocon is an oral immunomodulatory medication indicated for the treatment of adult patients with multiple myeloma, myelodysplastic syndromes that have a del(5q) cytogenetic abnormality, and mantle cell lymphoma, usually as part of combination chemotherapy protocols.

Lenalidomide binds to cereblon, a component of the CRL4‑E3 ubiquitin ligase complex, altering its substrate specificity. This triggers ubiquitination and proteasomal degradation of transcription factors Ikaros and Aiolos, leading to anti‑angiogenic effects, cytokine modulation, and enhanced immune‑mediated tumor cell killing.

The appropriate dose of Lenalidomide Biocon is determined by the prescribing healthcare professional based on the specific indication, disease stage, patient’s renal function, and concurrent therapies. No fixed dosing regimen is provided here; clinicians must individualise therapy.

Lenalidomide is classified as contraindicated in pregnancy because of potential teratogenic effects. Women of child‑bearing potential should use effective contraception, and breastfeeding is not recommended while receiving the drug. Consultation with a specialist is essential for risk assessment.

To order Lenalidomide Biocon, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.

Lenalidomide is a second‑generation analogue of thalidomide with a more favorable safety profile, especially regarding peripheral neuropathy. Compared with thalidomide, lenalidomide offers stronger anti‑angiogenic activity and greater immunomodulatory effects, while requiring similar monitoring for cytopenias and thrombotic risk.

Lenalidomide Biocon tablets should be stored at ambient temperature, below 25 °C, in the original blister pack or container. Protect the product from moisture, heat and direct sunlight to maintain potency throughout its shelf life.

Lenalidomide Biocon is administered orally, usually once daily in the evening with or without food, as directed by the treating physician. The tablets are swallowed whole with a glass of water and should not be crushed or chewed unless specifically advised.

The most serious risks include severe neutropenia, thrombocytopenia, thromboembolic events such as deep‑vein thrombosis or pulmonary embolism, secondary primary malignancies, and significant liver injury. Patients should be monitored regularly for blood counts, signs of clotting and liver function abnormalities.

Lenalidomide Biocon should not be used by patients with known hypersensitivity to lenalidomide or its excipients, by pregnant women, or by individuals with uncontrolled active infections. Caution is also advised for patients with severe renal impairment or those taking strong CYP3A4 inducers.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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