Product image of Lenalidomide Thornton & Ross Ltd. (Lenalidomide) supplied by GNH India

Lenalidomide Thornton & Ross Ltd.

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomide Thornton & Ross Ltd. (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomide Thornton & Ross Ltd., is an immunomodulatory drug presented as an oral formulation for systemic use. It is indicated for the treatment of multiple myeloma, myelodysplastic syndromes and mantle cell lymphoma in adult patients, often as part of combination therapy.

GNH India supplies Lenalidomide Thornton & Ross Ltd. as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide. The company adheres to EU GMP standards and provides secure logistics for regulated markets.

Manufacturer / TM Owner

Thornton & Ross Ltd

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Indications & Clinical Uses

  • Lenalidomide is used in hematologic malignancies that involve abnormal plasma or lymphoid cells.
  • Multiple Myeloma: improves survival and disease control when combined with other agents.
  • Myelodysplastic Syndromes with del(5q): reduces transfusion dependence and corrects cytopenias.
  • Mantle Cell Lymphoma: contributes to response rates in relapsed or refractory disease.

How It Works

  • Lenalidomide binds to the cereblon component of the CRL4‑E3 ubiquitin ligase complex, altering substrate specificity and promoting ubiquitination and proteasomal degradation of the transcription factors Ikaros (IKZF1) and Aiolos (IKZF3). This results in modulation of cytokine production, enhanced T‑ and NK‑cell immunity, inhibition of angiogenesis, and direct anti‑proliferative and pro‑apoptotic effects on malignant plasma and lymphoid cells.

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, sometimes accompanied by abdominal cramping.
  • Rash: mild skin erythema or itching.
  • Neutropenia: reduced neutrophil count, increasing infection risk.

Serious or Rare Side Effects

  • Thromboembolic events: deep vein thrombosis or pulmonary embolism.
  • Severe cutaneous reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Secondary primary malignancies: emergence of new cancers unrelated to the original disease.

Precautions & Warnings

When prescribing Lenalidomide, clinicians should observe several safety considerations.

  • Pregnancy risk: contraindicated in pregnancy (Category X); effective contraception required for both patient and partner.
  • Thromboembolism prophylaxis: assess need for anticoagulation in patients with additional risk factors.
  • Renal impairment: dose adjustment may be necessary in patients with reduced kidney function.
  • Hematologic monitoring: regular blood counts to detect neutropenia, anemia or thrombocytopenia.
  • Drug interactions: review concomitant medications, especially CYP3A4 inducers or inhibitors.
  • Store at ambient temperature: keep below 25 °C, in the original container, protected from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may markedly reduce plasma concentrations.
  • Anticoagulants (warfarin, direct oral anticoagulants): increased risk of bleeding when combined with thrombocytopenia.
  • Immunosuppressants (e.g., cyclosporine): heightened risk of severe neutropenia.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase exposure modestly.
  • P-glycoprotein substrates (e.g., digoxin): potential for altered levels.
  • Vaccines: live attenuated vaccines may be less effective; avoid during therapy.

Frequently Asked Questions

Lenalidomide is prescribed for adult patients with multiple myeloma, myelodysplastic syndromes that have a deletion of chromosome 5q, and mantle cell lymphoma, typically as part of a combination therapy regimen designed by the treating physician.

The drug binds to cereblon, a component of the CRL4‑E3 ubiquitin ligase complex, leading to the degradation of transcription factors Ikaros and Aiolos. This triggers immune modulation, anti‑angiogenic effects, and direct anti‑proliferative and pro‑apoptotic actions against malignant cells.

The specific dose and schedule of Lenalidomide are determined by the prescribing clinician based on the patient’s diagnosis, disease stage, renal function, and other individual factors. No standard dosing information is provided here.

Lenalidomide is classified as Pregnancy Category X, meaning it is contraindicated in pregnancy due to a high risk of fetal harm. Women of childbearing potential must use effective contraception, and breastfeeding is not recommended while on therapy.

To request Lenalidomide, 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 and offers a distinct mechanism compared with proteasome inhibitors or monoclonal antibodies. It is often combined with dexamethasone or other agents to enhance response rates, but the choice of therapy depends on disease characteristics and prior treatments.

Lenalidomide should be stored at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture and direct light, and ensure the container is tightly closed to maintain stability.

Lenalidomide is taken orally, usually as a tablet or capsule, with or without food as directed by the prescribing physician. The exact administration instructions, including timing relative to meals, are provided in the patient’s medication guide.

Serious risks include thromboembolic events such as deep‑vein thrombosis or pulmonary embolism, severe cutaneous reactions like Stevens‑Johnson syndrome, and the development of secondary primary malignancies. Patients should be monitored closely for signs of these conditions.

Lenalidomide is contraindicated in pregnant women and should not be used by individuals who cannot adhere to strict contraception requirements. Patients with uncontrolled infections, severe renal impairment without dose adjustment, or known hypersensitivity to the drug should also avoid its use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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