GNH USA

Europe — EMA

Irican

GNH USA supplies Irican (Irinotecan), a topoisomerase I inhibitor for metastatic colorectal cancer, adjuvant colon cancer and small cell lung cancer.

Irinotecan Hydrochloride Trihydrate

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What is Irinotecan Hydrochloride Trihydrate?

Irinotecan, the active ingredient in Irican, is a topoisomerase I inhibitor presented as an intravenous formulation for use in oncology patients. It is employed in the treatment of certain advanced solid tumours and as adjuvant therapy in colon cancer. GNH USA supplies Irican as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

What is Irinotecan Hydrochloride Trihydrate used for?

Irican belongs to the topoisomerase I inhibitor class and is used in cancers that rely on rapid DNA replication. - Metastatic colorectal cancer: improves overall survival when combined with fluoropyrimidine‑based regimens. - Adjuvant treatment of colon cancer: reduces risk of disease recurrence after surgical resection. - Small cell lung cancer: provides therapeutic benefit as part of combination chemotherapy protocols.

What are the side effects of Irinotecan Hydrochloride Trihydrate?

Irinotecan is associated with a range of adverse reactions that vary in frequency and severity.

Common Side Effects: - Diarrhea: often delayed and may be severe. - Nausea and vomiting: typically manageable with anti‑emetics. - Neutropenia: reduced white blood cell count increasing infection risk. - Alopecia: temporary hair loss. - Fatigue: generalized tiredness during treatment cycles.

Serious or Rare Side Effects: - Febrile neutropenia: fever with low neutrophil count requiring urgent care. - Severe colitis or bowel perforation: life‑threatening gastrointestinal complications. - Anaphylactic reactions: rare but may occur during infusion. - Hepatotoxicity: elevated liver enzymes indicating liver injury.

What precautions apply to Irinotecan Hydrochloride Trihydrate?

Before initiating Irican therapy, clinicians should assess patient‑specific factors and monitor for toxicity. - Monitor blood counts: perform regular complete blood count to detect neutropenia. - Assess liver function: adjust dosing in hepatic impairment. - Evaluate bowel status: avoid use in patients with recent abdominal surgery or obstruction. - Use anti‑emetics prophylactically: to reduce nausea and vomiting. - Adjust dose for UGT1A1 polymorphisms: consider genetic testing where available. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

What does Irinotecan Hydrochloride Trihydrate interact with?

Irinotecan may interact with other medicines that affect its metabolism or increase toxicity.

Major Interactions (Avoid): - Strong CYP3A4 inducers (e.g., rifampin): may markedly reduce irinotecan exposure. - UGT1A1 inhibitors (e.g., atazanavir): can increase SN‑38 levels and risk of severe neutropenia. - Concurrent myelosuppressive agents: heighten risk of bone‑marrow suppression.

Moderate Interactions (Monitor Closely): - Moderate CYP3A4 inhibitors (e.g., fluconazole): may modestly increase exposure. - Anticoagulants (e.g., warfarin): monitor coagulation parameters due to potential bleeding risk. - NSAIDs or aspirin: may exacerbate gastrointestinal toxicity.

Frequently asked questions

What conditions is Irican used to treat?+
Irican (irinotecan) is indicated for metastatic colorectal cancer, as adjuvant therapy after colon cancer surgery, and for small cell lung cancer. In each case it is used as part of a combination chemotherapy regimen to improve survival outcomes.
How does irinotecan work in the body?+
Irinotecan is converted inside tumour cells to the active metabolite SN‑38, which inhibits topoisomerase I. This enzyme normally relieves DNA supercoiling during replication; its inhibition leads to persistent single‑strand breaks, DNA damage, and ultimately tumour cell death.
What is the usual dose of Irican?+
The dose of Irican is determined individually by the prescribing oncologist based on the specific cancer type, treatment protocol, patient weight, liver function, and other clinical factors. Only a qualified healthcare professional should set the dosing schedule.
Is Irican safe to use during pregnancy or breastfeeding?+
Irinotecan is classified as contraindicated in pregnancy because it can cause fetal harm. It is also not recommended during breastfeeding, as it may be excreted in milk and affect the infant. Women of child‑bearing potential should use effective contraception.
How do I order Irican from GNH USA?+
To request Irican, submit an enquiry on the product page at gnh-usa.com specifying the required quantity. GNH USA works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where needed) and necessary import documentation.
How does Irican compare with other topoisomerase I inhibitors?+
Irican (irinotecan) is the most widely used topoisomerase I inhibitor in colorectal and small cell lung cancer. Compared with alternatives such as topotecan, irinotecan generally offers a broader spectrum of activity in solid tumours but may have a higher incidence of delayed diarrhea and neutropenia, requiring specific supportive care.
What are the storage requirements for Irican?+
Irican should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the product in its original packaging until preparation to maintain stability.
How is Irican administered to patients?+
Irican is given by intravenous infusion, typically over 30‑90 minutes depending on the protocol. The infusion is performed in a clinical setting by qualified healthcare staff, with monitoring for infusion‑related reactions and vital signs throughout the administration.
What are the most serious risks associated with Irican therapy?+
The most serious risks include severe neutropenia with fever (febrile neutropenia), life‑threatening delayed diarrhea, bowel perforation, and rare anaphylactic reactions. Prompt recognition and supportive measures are essential to manage these complications.
Who should not receive Irican?+
Irican is contraindicated in patients with known hypersensitivity to irinotecan or its excipients, those with uncontrolled infections, severe hepatic impairment, or active bowel obstruction. Caution is also advised for patients with UGT1A1 deficiency, as they may experience heightened toxicity.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Irinotecan Hydrochloride Trihydrate
Route
Intravenous Use
Manufacturer
Ariti Sa
Origin
EU

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