Product image of Igos (Arsenic Trioxide) supplied by GNH India

Igos

Active Ingredient:
Arsenic Trioxide
Origin:
EU

Igos (Arsenic Trioxide)

Arsenic trioxide, the active ingredient in Igos, is an antineoplastic agent presented as a sterile solution for intravenous use. It is employed in the treatment of acute promyelocytic leukemia, targeting malignant promyelocytes in adult patients.
GNH India supplies Igos as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

Igos (arsenic trioxide) is used within the acute promyelocytic leukemia (APL) therapeutic pathway to achieve disease control.

  • Acute promyelocytic leukemia (newly diagnosed): induces remission by promoting differentiation of leukemic cells.
  • Acute promyelocytic leukemia (relapsed or refractory): provides disease control when standard therapy has failed.
  • High‑risk acute promyelocytic leukemia: contributes to differentiation therapy as part of combination regimens.

How It Works

  • Arsenic trioxide binds to the PML‑RARA oncoprotein, triggering its degradation and thereby releasing the transcriptional block that prevents promyelocyte maturation. This degradation induces apoptosis and partial differentiation of leukemic cells, restoring normal hematopoietic development and reducing the leukemic burden in acute promyelocytic leukemia.

Side Effects

Arsenic trioxide may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Fatigue: generalized tiredness during therapy.
  • Fever: transient elevations in body temperature.
  • Headache: mild to moderate intensity.
  • Constipation: reduced bowel movements.
  • Mild QT interval prolongation: detectable on ECG monitoring.

Serious or Rare Side Effects

  • Differentiation syndrome: potentially life‑threatening inflammatory response.
  • Severe QT prolongation: risk of torsades de pointes arrhythmia.
  • Hepatic toxicity: elevated liver enzymes or hepatic dysfunction.
  • Renal failure: impaired kidney function requiring monitoring.
  • Severe infection: opportunistic infections due to immunosuppression.
  • Leukocytosis: rapid rise in white blood cell count.

Precautions & Warnings

When using Igos, clinicians should observe specific safety measures to minimize risk.

  • Cardiac monitoring: perform baseline and periodic ECGs to detect QT prolongation.
  • Electrolyte management: correct potassium and magnesium deficits before infusion.
  • Hepatic function: assess liver enzymes and adjust therapy if significant impairment exists.
  • Pregnancy considerations: avoid use in pregnant women unless benefits outweigh potential risks.
  • Differentiation syndrome vigilance: monitor for fever, weight gain, respiratory distress, and intervene promptly.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Arsenic trioxide can interact with other medicines, altering safety or efficacy.

Major Interactions (Avoid)

  • QT‑prolonging agents (e.g., quinidine, sotalol): increase risk of dangerous arrhythmias.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may raise arsenic levels.
  • Azole antifungals: potentiate toxicity through metabolic inhibition.

Moderate Interactions (Monitor Closely)

  • All‑trans retinoic acid (ATRA): heightened risk of differentiation syndrome; monitor closely.
  • Diuretics: may exacerbate electrolyte disturbances; check serum potassium and magnesium.
  • Electrolyte supplements: adjust dosing to avoid over‑correction of potassium/magnesium.

Frequently Asked Questions

Igos contains arsenic trioxide and is used as an antineoplastic agent for the treatment of acute promyelocytic leukemia (APL). It works as part of a differentiation therapy regimen to induce remission in newly diagnosed or relapsed APL patients.

Arsenic trioxide targets the PML‑RARA fusion protein that drives APL. By binding to this oncoprotein, it promotes its degradation, which releases the block on cell differentiation and triggers programmed cell death, thereby reducing the leukemic cell population.

The dosing regimen for Igos is determined by the treating physician based on the patient’s clinical status, disease phase, and laboratory parameters. Prescribers calculate the appropriate infusion rate and total dose according to established guidelines.

The safety of arsenic trioxide in pregnancy and lactation has not been established. It is generally avoided unless the potential benefit to the mother outweighs the possible risk to the fetus or infant, and it should be used only under specialist supervision.

To order Igos, 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 (including cold‑chain where required) and necessary import documentation.

Igos (arsenic trioxide) is often combined with all‑trans retinoic acid (ATRA) and is considered comparable to other differentiation‑based regimens. Compared with conventional chemotherapy, arsenic trioxide offers a targeted mechanism with a distinct side‑effect profile, especially regarding cardiac monitoring and differentiation syndrome.

Igos must be stored refrigerated at 2‑8 °C, protected from light, and should never be frozen or shaken. Prior to administration, the solution should be inspected for particulate matter and used within the time frame specified by the manufacturer.

Igos is supplied as a sterile intravenous solution. It is administered by slow infusion under continuous cardiac monitoring, typically in a hospital or oncology centre, with electrolyte levels checked before and during treatment.

The most serious risks include differentiation syndrome, severe QT interval prolongation leading to arrhythmias, hepatic toxicity, renal failure, and life‑threatening infections. Early detection and prompt management of these events are essential for patient safety.

Igos is contraindicated in patients with known hypersensitivity to arsenic trioxide, those with uncontrolled prolonged QT interval, severe hepatic or renal impairment, and in pregnant women unless the therapeutic benefit justifies the potential risk.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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