Product image of Hasgobusno (Cabozantinib) supplied by GNH India

Hasgobusno

Active Ingredient:
Cabozantinib
Origin:
EU

Hasgobusno (Cabozantinib)

Hasgobusno is a prescription oral medication whose active ingredient is cabozantinib, a tyrosine kinase inhibitor used in oncology. The product is marketed in the European Union, but specific dosage form and strength are not disclosed in the available data. Cabozantinib works by blocking multiple receptor tyrosine kinases involved in tumor growth and angiogenesis. It is classified under ATC code L01XE02 and is prescribed for certain advanced cancers.

Manufacturer / TM Owner

Day Zero Ehf

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Indications & Clinical Uses

Hasgobusno (cabozantinib) is indicated for the treatment of several advanced solid tumors in adult patients.

  • Metastatic renal cell carcinoma (RCC) after prior therapy.
  • Unresectable or metastatic hepatocellular carcinoma (HCC) in patients who have received prior sorafenib.
  • Progressive medullary thyroid cancer (MTC) in patients with documented disease progression.
  • Off‑label use in certain other tyrosine‑kinase driven cancers as determined by a physician.
  • Combination therapy with other targeted agents may be considered in clinical trials.
  • Use in pediatric populations is not established and should be limited to clinical study settings.

Side Effects

The safety profile of Hasgobusno reflects the pharmacologic activity of cabozantinib and includes both common and less frequent serious adverse events that clinicians monitor closely.

Common

  • Diarrhea, often mild to moderate and may be managed with antidiarrheal medication.
  • Nausea or vomiting, which can be alleviated with anti‑emetic agents.
  • Fatigue, commonly reported and may affect daily activities.
  • Hand‑foot syndrome (palmar‑plantar erythrodysesthesia), presenting as redness, swelling, or pain on the palms or soles.

Serious

  • Hypertension, which can be severe and may require antihypertensive therapy.
  • Gastrointestinal perforation or fistula, a rare but serious condition requiring immediate medical attention.
  • Hemorrhage, including pulmonary hemorrhage, which can be life‑threatening.

Precautions & Warnings

Precautions for Hasgobusno focus on patient selection, monitoring, and management of potential risks associated with its mechanism of action.

  • Assess baseline blood pressure and cardiovascular status before initiating therapy.
  • Monitor liver function tests regularly and carefully during treatment.
  • Evaluate for signs of gastrointestinal bleeding or perforation.
  • Perform periodic complete blood counts to regularly detect cytopenias.
  • Counsel patients on the risk of hand‑foot syndrome and advise skin care measures.
  • Advise women of childbearing potential to use effective contraception and discuss pregnancy risks.

Avoid Interactions

Cabozantinib may interact with several drug classes, influencing its plasma concentration or increasing the risk of adverse events.

Avoid

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine) that can reduce cabozantinib exposure.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin) that may increase drug levels and toxicity.
  • Concurrent use with other potent anti‑angiogenic agents due to additive risk of hypertension and bleeding.

Use with caution

  • Anticoagulants and antiplatelet drugs, which may heighten bleeding risk.
  • Proton pump inhibitors, which can affect gastric pH and possibly alter absorption.
  • CYP3A4 substrates with narrow therapeutic windows, requiring dose adjustments and close monitoring.

Frequently Asked Questions

Hasgobusno contains the active ingredient cabozantinib, which is a tyrosine kinase inhibitor used to treat certain advanced cancers.

It is prescribed for metastatic renal cell carcinoma, unresectable or metastatic hepatocellular carcinoma after prior sorafenib, and progressive medullary thyroid cancer.

Hasgobusno is taken orally as a prescription medication; the exact dosage form and strength are defined by the prescribing physician.

Common side effects include diarrhea, nausea or vomiting, fatigue, and hand‑foot syndrome (palmar‑plantar erythrodysesthesia).

Serious events such as severe hypertension, gastrointestinal perforation or fistula, and pulmonary hemorrhage should be evaluated promptly.

Regular monitoring of blood pressure, liver function tests, complete blood counts, and assessment for gastrointestinal bleeding is recommended.

Combination with other targeted agents may be considered in clinical trials, but concurrent use with other anti‑angiogenic drugs should be avoided.

Strong CYP3A4 inducers (e.g., rifampin) and strong CYP3A4 inhibitors (e.g., ketoconazole) should be avoided because they can alter cabozantinib levels.

Anticoagulants and antiplatelet agents can increase bleeding risk, so they should be used only with caution and close monitoring.

Women should use effective contraception and discuss potential pregnancy risks with their healthcare provider before starting Hasgobusno.

Cabozantinib can cause elevations in liver enzymes; regular liver function testing is recommended during therapy.

Additional details can be obtained from the prescribing information, the European Medicines Agency, or a qualified healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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