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

Lenalidomide Clonmel

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomide Clonmel (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomide Clonmel, is a immunomodulatory imide drug (IMiD) presented as an oral tablet for oral use. It treats multiple myeloma, myelodysplastic syndromes with del(5q), and mantle cell lymphoma in appropriate patients.

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

Manufacturer / TM Owner

Clonmel Healthcare Ltd.

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Indications & Clinical Uses

  • Lenalidomide is an immunomodulatory agent used in hematologic malignancies and related disorders.
  • Multiple Myeloma: improves progression‑free survival and overall response in patients with relapsed or refractory disease.
  • Myelodysplastic Syndromes with del(5q): reduces transfusion dependence and can induce cytogenetic remission.
  • Mantle Cell Lymphoma: contributes to disease control when used in combination regimens.

How It Works

  • Lenalidomide binds to the cereblon component of the CRL4‑E3 ubiquitin ligase complex, altering substrate specificity and promoting degradation of transcription factors Ikaros (IKZF1) and Aiolos (IKZF3). This results in modulation of cytokine production, inhibition of angiogenesis, and direct anti‑tumor activity through apoptosis and cell‑cycle arrest in malignant cells.

Side Effects

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

Common Side Effects

  • Fatigue: persistent tiredness reported by many patients.
  • Neutropenia: reduced neutrophil count increasing infection risk.
  • Thrombocytopenia: lowered platelet levels that may cause bruising.
  • Diarrhea: loose stools that may require supportive care.

Serious or Rare Side Effects

  • Venous thromboembolism: deep vein thrombosis or pulmonary embolism.
  • Severe neutropenia: profound immune suppression leading to serious infections.
  • Secondary primary malignancies: emergence of new cancers.
  • Hepatic toxicity: elevated liver enzymes or liver injury.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Cardiac events: arrhythmias or myocardial infarction in rare cases.

Precautions & Warnings

  • Before initiating therapy, several safety considerations should be addressed.
  • Pregnancy: contraindicated (Category X); avoid use in pregnant women.
  • Thrombosis risk: assess patient history and consider prophylactic anticoagulation.
  • Hematologic monitoring: perform regular complete blood counts to detect cytopenias.
  • Renal impairment: evaluate kidney function and adjust dose if necessary.
  • Store at ambient temperature: keep below 25 °C, protect from moisture and light in the original container.

Avoid Interactions

Lenalidomide can interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may markedly reduce lenalidomide exposure.
  • Anticoagulants (e.g., warfarin): increased risk of thromboembolic events when combined.
  • Live vaccines: heightened risk of infection due to immunosuppression.
  • Hormonal contraceptives: reduced efficacy; alternative contraception advised.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): may increase drug levels.
  • Immunosuppressants (e.g., cyclosporine, tacrolimus): additive infection risk.
  • Other myelosuppressive agents (e.g., chemotherapy, azacitidine): may exacerbate bone‑marrow suppression.
  • NSAIDs: potential for increased renal toxicity in susceptible patients.

Frequently Asked Questions

Lenalidomide Clonmel is indicated for the treatment of multiple myeloma, myelodysplastic syndromes with deletion 5q, and mantle cell lymphoma. In each condition it is used to control disease progression, improve response rates, and reduce the need for blood transfusions where applicable.

Lenalidomide binds to cereblon, a component of the CRL4‑E3 ubiquitin ligase complex, leading to degradation of transcription factors Ikaros and Aiolos. This triggers immune modulation, anti‑angiogenic effects, and direct anti‑tumor activity by promoting apoptosis and inhibiting proliferation of malignant cells.

The dose of Lenalidomide Clonmel is individualized and determined by the prescribing clinician based on the specific indication, disease stage, renal function, and patient tolerance. Patients should follow the dosing schedule provided by their healthcare professional.

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 during breastfeeding because it may be excreted in milk and could affect the infant.

To order Lenalidomide Clonmel, 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 shares the same class as thalidomide and pomalidomide but generally offers a more favorable safety profile than thalidomide, especially regarding peripheral neuropathy. Compared with pomalidomide, lenalidomide is often used earlier in therapy and has a broader label for myelodysplastic syndromes with del(5q). Choice of agent depends on disease, prior therapy and individual patient factors.

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

Lenalidomide is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water and not crushed, chewed, or split unless specifically instructed by a healthcare professional.

The most serious risks include venous thromboembolism, severe neutropenia or other cytopenias that can lead to infection, secondary primary malignancies, and significant liver toxicity. Patients should be monitored regularly for signs of blood clots, infections, abnormal liver tests, and new cancer development.

Lenalidomide should not be used by pregnant women, individuals with known hypersensitivity to the drug, patients with uncontrolled active infections, or those with severe renal impairment without appropriate dose adjustment. It is also contraindicated in patients receiving live vaccines.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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