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

Lenalidomide Stragen

Active Ingredient:
Lenalidomide
Origin:
EU

Lenalidomide Stragen (Lenalidomide)

Lenalidomide, the active ingredient in Lenalidomide Stragen, is an immunomodulatory drug (IMiD) presented as an oral formulation for oral use. It is employed in the treatment of certain hematologic malignancies, specifically multiple myeloma and myelodysplastic syndromes, in adult patients.

GNH India supplies Lenalidomide Stragen as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide, ensuring quality and regulatory compliance across global markets and providing reliable logistics for timely delivery.

Manufacturer / TM Owner

Stragen France

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Indications & Clinical Uses

  • Lenalidomide is used in hematologic oncology to target malignant plasma cells and dysplastic bone‑marrow clones.
  • Multiple Myeloma: improves progression‑free and overall survival in patients with relapsed or refractory disease.
  • Myelodysplastic Syndromes: reduces transfusion dependence and delays progression to acute leukemia.
  • Myelodysplastic Syndrome with del(5q) deletion: corrects anemia and decreases need for red‑cell support.

How It Works

  • Lenalidomide binds to cereblon, a component of the CRL4‑CRBN E3 ubiquitin ligase complex, altering substrate specificity and promoting degradation of transcription factors such as Ikaros and Aiolos. This leads to modulation of cytokine production, inhibition of angiogenesis, and induction of apoptosis in malignant cells, while enhancing natural killer and T‑cell mediated immune responses.

Side Effects

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

Common Side Effects

  • Fatigue: persistent tiredness affecting daily activities.
  • Neutropenia: reduced neutrophil count increasing infection risk.
  • Thrombocytopenia: low platelet levels leading to easy bruising.
  • Anemia: decreased red blood cells causing weakness.
  • Diarrhea: loose stools that may require hydration.
  • Rash: skin irritation or redness.

Serious or Rare Side Effects

  • Venous thromboembolism: blood clots in deep veins or lungs.
  • Severe neutropenia: profound infection susceptibility.
  • Severe thrombocytopenia: risk of serious bleeding.
  • Secondary primary malignancies: emergence of new cancers.
  • Severe liver injury: marked elevation of hepatic enzymes.
  • Hypersensitivity reactions: including anaphylaxis.

Precautions & Warnings

  • Before initiating therapy, clinicians should evaluate specific safety considerations.
  • Pregnancy Contraindication: Lenalidomide is teratogenic and must not be used during pregnancy.
  • Thrombosis Risk: Assess patient history and consider prophylactic anticoagulation when appropriate.
  • Blood Count Monitoring: Perform regular CBCs to detect cytopenias early.
  • Renal Impairment: Adjust dosing in patients with reduced kidney function.
  • Hepatic Impairment: Use caution in severe liver disease.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole): may increase exposure.
  • Strong CYP3A4 inducers (e.g., rifampin): may reduce efficacy.
  • Anticoagulants (e.g., warfarin): heightened risk of bleeding.

Moderate Interactions (Monitor Closely)

  • NSAIDs: additive risk of gastrointestinal bleeding.
  • CYP3A4 substrates (e.g., midazolam): may require dose adjustment.

Frequently Asked Questions

Lenalidomide Stragen is indicated for the treatment of adult patients with multiple myeloma and for myelodysplastic syndromes, including those with a del(5q) cytogenetic abnormality. It is prescribed to control disease progression and reduce transfusion requirements.

Lenalidomide binds to the cereblon component of the CRL4‑CRBN E3 ubiquitin ligase, altering the degradation of specific transcription factors. This results in immune modulation, anti‑angiogenic effects, and induction of apoptosis in malignant cells, while enhancing natural killer and T‑cell activity.

The dosage of Lenalidomide Stragen is individualized by the prescribing clinician based on the patient’s diagnosis, disease stage, renal function, and other clinical factors. Only a qualified healthcare professional can determine the appropriate regimen.

Lenalidomide is classified as Pregnancy Category X because it is highly teratogenic. It must not be used by pregnant women or women who may become pregnant. Breastfeeding is also contraindicated, as the drug can be excreted in milk and harm the infant.

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.

Both lenalidomide and thalidomide belong to the immunomodulatory drug class, but lenalidomide has a more favorable safety profile, especially regarding peripheral neuropathy, and exhibits stronger anti‑angiogenic and anti‑myeloma activity. Clinical guidelines often prefer lenalidomide for relapsed or refractory multiple myeloma.

Lenalidomide Stragen should be stored at ambient temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the product out of reach of children and avoid storing in humid environments such as bathrooms.

The medication is taken orally, usually as a tablet, with or without food as directed by the prescriber. Patients should swallow the tablet whole with water and follow the dosing schedule provided by their healthcare professional.

The most serious risks include severe neutropenia, thrombocytopenia, venous thromboembolism, secondary primary malignancies, and life‑threatening hypersensitivity reactions. Regular monitoring of blood counts and vigilance for signs of clotting or infection are essential during therapy.

Lenalidomide is contraindicated in pregnant women, women who may become pregnant, and patients with known hypersensitivity to lenalidomide or any component of the formulation. Caution is also advised for individuals with severe renal or hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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