GNH USA

Europe — EMA

Irinotecan Kabi

GNH USA supplies Irinotecan Kabi (Irinotecan), a topoisomerase I inhibitor for metastatic and advanced colorectal cancer. Request a quote for global supply.

Irinotecan Hydrochloride Trihydrate

Request sourcing

1
Pack/s

What is Irinotecan Hydrochloride Trihydrate?

Irinotecan Hydrochloride Trihydrate, the active ingredient in Irinotecan Kabi, is a topoisomerase I inhibitor presented as an intravenous formulation for use in oncology. It is employed in the treatment of metastatic and advanced colorectal cancer and may be incorporated into combination regimens for other solid tumors.

GNH USA supplies Irinotecan Kabi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

What is Irinotecan Hydrochloride Trihydrate used for?

Irinotecan Kabi is used in chemotherapy regimens targeting colorectal cancer and other solid tumors. - Metastatic colorectal cancer: improves progression‑free survival when combined with other agents. - Advanced colorectal cancer: used as part of first‑line or second‑line therapy to reduce tumor burden. - Other solid tumors (e.g., gastric, pancreatic): incorporated into combination protocols to enhance cytotoxic effect.

What are the side effects of Irinotecan Hydrochloride Trihydrate?

Irinotecan Kabi may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects: - Diarrhea: often severe and may require antidiarrheal therapy. - Nausea and vomiting: may be managed with anti‑emetics. - Neutropenia: reduced white blood cell count increasing infection risk. - Fatigue: general tiredness affecting daily activities.

Serious or Rare Side Effects: - Febrile neutropenia: fever with low neutrophil count, a medical emergency. - Intestinal perforation: rare but life‑threatening bowel rupture. - Severe hypersensitivity reactions: including anaphylaxis, requiring immediate treatment.

What precautions apply to Irinotecan Hydrochloride Trihydrate?

When using Irinotecan Kabi, clinicians should observe several safety precautions to minimize risks. - Baseline blood counts: obtain CBC before each cycle to monitor neutropenia. - Liver function: assess hepatic enzymes as metabolism may be impaired. - Hydration: ensure adequate fluid intake to reduce risk of severe diarrhea. - Drug interactions: avoid concurrent strong CYP3A4 inhibitors that can increase SN‑38 exposure. - Pregnancy and lactation: contraindicated unless benefits outweigh unknown risks; discuss with specialist. - Store at ambient temperature: keep vials below 25 °C, protect from light, and retain in original packaging.

What does Irinotecan Hydrochloride Trihydrate interact with?

Irinotecan Kabi can interact with other medicines, altering its efficacy or toxicity.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, ritonavir): may raise SN‑38 levels, increasing toxicity. - UGT1A1 inhibitors (e.g., atazanavir): can reduce SN‑38 glucuronidation, heightening risk of neutropenia and diarrhea. - Concurrent use with other myelosuppressive agents: can exacerbate bone‑marrow suppression.

Moderate Interactions (Monitor Closely): - Anticoagulants (e.g., warfarin): monitor INR as irinotecan may affect coagulation. - Antidiarrheal agents (e.g., loperamide): adjust dosing to avoid masking severe diarrhea. - Radiotherapy to abdomen/pelvis: increased gastrointestinal toxicity may occur.

Frequently asked questions

What is Irinotecan Kabi used for?+
Irinotecan Kabi is indicated for the treatment of metastatic and advanced colorectal cancer and may be used as part of combination chemotherapy regimens for other solid tumors such as gastric or pancreatic cancer. It is administered under the supervision of an oncologist as part of a systemic cancer therapy plan.
How does Irinotecan work?+
Irinotecan is a pro‑drug that is converted inside tumor cells to the active metabolite SN‑38. SN‑38 binds to the DNA‑topoisomerase I enzyme, preventing the re‑ligation of single‑strand DNA breaks during replication. This leads to accumulation of DNA damage, triggering apoptosis and cell death in rapidly dividing cancer cells.
What is the usual dose of Irinotecan Kabi?+
The dose of Irinotecan Kabi is individualized and determined by the prescribing oncologist based on factors such as the type of cancer, treatment regimen, patient weight, liver function and prior therapy. No standard dose is provided here; the prescriber will calculate the appropriate amount for each patient.
Is Irinotecan safe during pregnancy or breastfeeding?+
The safety of Irinotecan in pregnancy and lactation has not been established. It is generally avoided unless the potential benefit to the mother outweighs the unknown risk to the fetus or infant. Women of child‑bearing potential should use effective contraception during treatment and for a period thereafter as advised by their physician.
How do I order Irinotecan Kabi from GNH USA?+
To order Irinotecan Kabi, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams across international markets. After the request, the sales team will verify trade or institutional credentials, then provide pricing, availability, shipping details (including any cold‑chain requirements) and assist with import documentation.
How does Irinotecan compare with its main alternative drug or class?+
The primary alternative to Irinotecan in colorectal cancer regimens is the topoisomerase I inhibitor topotecan, though topotecan is less commonly used for this indication. Compared with oxaliplatin‑based regimens, Irinotecan offers a different toxicity profile, with more pronounced gastrointestinal effects but less peripheral neuropathy. Choice of therapy depends on prior treatment history, patient tolerance and molecular characteristics of the tumor.
How should Irinotecan Kabi be stored and handled?+
Irinotecan Kabi vials should be stored at ambient temperature, preferably below 25 °C, protected from light and moisture. Keep the product in its original packaging until use. Do not freeze. Follow standard aseptic techniques when preparing the intravenous infusion to maintain sterility.
How is Irinotecan Kabi given or administered?+
Irinotecan Kabi is administered by intravenous infusion, typically over 30 to 90 minutes depending on the protocol. The infusion schedule (e.g., weekly, bi‑weekly) and total treatment cycle are defined by the treating oncologist based on the specific cancer type, combination partners and patient response.
What are the most serious risks to watch for with Irinotecan?+
The most serious risks associated with Irinotecan include severe neutropenia leading to infection, febrile neutropenia, life‑threatening diarrhea that may cause dehydration, intestinal perforation, and rare but severe hypersensitivity reactions such as anaphylaxis. Patients should be monitored closely for signs of infection, fever, persistent diarrhea or abdominal pain, and any allergic symptoms.
Who should not use Irinotecan Kabi?+
Irinotecan Kabi should be avoided in patients with known hypersensitivity to irinotecan or any of its excipients, those with severe hepatic impairment, and individuals with uncontrolled infections. Caution is also advised for patients with pre‑existing severe bone‑marrow suppression or gastrointestinal disorders that could be aggravated by the drug.
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
Fresenius Kabi Nv/Sa
Origin
EU

Related products