Product image of Imatinib Aspire (Imatinib) supplied by GNH India

Imatinib Aspire

Active Ingredient:
Imatinib
Origin:
EU

Imatinib Aspire (Imatinib)

Imatinib, the active ingredient in Imatinib Aspire, is a tyrosine kinase inhibitor presented as an oral formulation for oral use. It treats chronic myeloid leukemia and gastrointestinal stromal tumor in adult patients.

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

Manufacturer / TM Owner

Aspire Pharma Limited

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Indications & Clinical Uses

  • Imatinib Aspire targets BCR‑ABL driven malignancies and related tyrosine‑kinase pathways.
  • Chronic Myeloid Leukemia (CML): reduces leukemic cell proliferation and improves long‑term survival.
  • Gastrointestinal Stromal Tumor (GIST): inhibits tumor growth and delays disease progression.
  • Philadelphia chromosome‑positive Acute Lymphoblastic Leukemia (Ph+ ALL): provides targeted inhibition of leukemic blasts.

How It Works

  • Imatinib binds competitively to the ATP‑binding site of the BCR‑ABL tyrosine kinase, as well as c‑KIT and PDGFR, blocking phosphorylation cascades that drive malignant cell proliferation and survival. This inhibition halts downstream signaling pathways, leading to apoptosis of abnormal cells and tumor growth control.

Side Effects

Imatinib Aspire may cause a range of adverse reactions.

Common Side Effects

  • Nausea or vomiting
  • Fluid retention or peripheral edema
  • Muscle cramps or weakness
  • Fatigue or tiredness
  • Diarrhea or abdominal discomfort
  • Skin rash or pruritus

Serious or Rare Side Effects

  • Severe neutropenia or leukopenia
  • Hepatotoxicity with elevated liver enzymes
  • Cardiac failure or reduced left‑ventricular function
  • Pulmonary arterial hypertension
  • Stevens‑Johnson syndrome or toxic epidermal necrolysis
  • Tumor lysis syndrome in high‑burden disease

Precautions & Warnings

  • Before initiating therapy, clinicians should assess baseline parameters and monitor patients regularly.
  • Monitor blood counts: perform complete blood count at baseline and periodically.
  • Assess liver function: check hepatic enzymes before and during treatment.
  • Evaluate cardiac status: perform echocardiogram if there is a history of heart disease.
  • Avoid in patients with known hypersensitivity to imatinib or its excipients.
  • Use caution in severe renal or hepatic impairment: dose adjustment may be required.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Imatinib can interact with several concomitant medicines, altering its efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase imatinib plasma levels.
  • Potent CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce therapeutic exposure.
  • Concomitant use with antacids containing aluminum or magnesium: can decrease absorption.

Moderate Interactions (Monitor Closely)

  • Warfarin: imatinib may enhance anticoagulant effect; monitor INR.
  • Diuretics (e.g., furosemide): increased risk of fluid retention.
  • QT‑prolonging agents (e.g., sotalol): monitor cardiac rhythm and electrolytes.

Frequently Asked Questions

Imatinib Aspire is a prescription‑only oral medication indicated for the treatment of chronic myeloid leukemia (CML) and gastrointestinal stromal tumor (GIST). It may also be used in Philadelphia chromosome‑positive acute lymphoblastic leukemia, where it targets the BCR‑ABL fusion protein that drives malignant cell growth.

Imatinib inhibits the ATP‑binding site of the BCR‑ABL tyrosine kinase as well as c‑KIT and PDGFR receptors. By blocking these enzymes, it prevents downstream signaling that promotes uncontrolled cell division, leading to reduced proliferation of leukemic and tumor cells and ultimately inducing apoptosis.

The exact dose of Imatinib Aspire is individualized by the treating physician based on the specific indication, disease stage, patient weight, renal and hepatic function, and response to therapy. Only a qualified prescriber should set the dosing regimen.

Safety data for Imatinib during pregnancy and lactation are limited. It is generally advised to avoid use unless the potential benefit outweighs the risk to the fetus or infant. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternatives with their healthcare provider.

To place an order, submit an enquiry on the Imatinib Aspire 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 (including any cold‑chain requirements) and necessary import documentation.

Imatinib was the first BCR‑ABL tyrosine‑kinase inhibitor approved for CML and remains a standard first‑line option. Newer TKIs such as dasatinib and nilotinib offer alternative potency and side‑effect profiles, but Imatinib is often preferred for its long‑term safety data and cost‑effectiveness in many health‑care settings.

Imatinib Aspire should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight, and excessive heat to maintain stability throughout its shelf life.

Imatinib Aspire is taken orally, usually once daily, with a glass of water. It can be swallowed with or without food, although taking it with a meal may reduce gastrointestinal discomfort for some patients.

Patients should be alert for severe neutropenia or leukopenia, signs of liver injury (jaundice, dark urine), cardiac dysfunction (shortness of breath, swelling), pulmonary hypertension, and rare but serious skin reactions such as Stevens‑Johnson syndrome. Prompt medical evaluation is essential if any of these occur.

Imatinib Aspire is contraindicated in individuals with known hypersensitivity to imatinib or any of its excipients. Caution is also advised for patients with severe hepatic impairment, uncontrolled heart failure, or those receiving strong CYP3A4 inducers that could markedly lower drug exposure.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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