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Kanjinti: Benefits, Reviews, Info, Side Effects!
Rx Details
Kanjinti
Trastuzumab, Herceptin, Ogivri, Ontruzant
Trastuzumab-anns
Prescription
Biosimilar
Drugs
Biosimilar
biosimilar to Herceptin, treats HER2-positive breast cancer, used in combination with other cancer treatments, may improve survival rates, may reduce risk of cancer recurrence, generally well-tolerated, cost-effective alternative
Chills, Cough, Diarrhea, Fatigue, Fever, Headache, Heart Problems, Infection, Joint Pain, Low White Blood Cell Count, Muscle Pain, Nausea, Rash, Shortness Of Breath, Weakness
Kanjinti is a biosimilar to Herceptin (trastuzumab) and is used in the treatment of HER2-positive breast cancer and gastric cancer. The dosage of Kanjinti, like Herceptin, depends on the specific treatment regimen and the condition being treated. For breast cancer, the typical initial dose is 8 mg/kg administered as an intravenous infusion, followed by subsequent doses of 6 mg/kg every three weeks. For gastric cancer, the initial dose is usually 8 mg/kg, followed by 6 mg/kg every three weeks. However, the exact dosage and schedule can vary based on individual patient factors and the specific treatment plan prescribed by a healthcare provider. It is important to follow the guidance of a healthcare professional for the appropriate dosage and administration.
Her2-positive breast cancer, her2-positive gastric cancer
Similar safety profile to Herceptin.
No interactions found
$1,000 – $2,000
$1,500

A Synopsis of

Kanjinti

Kanjinti is a medication that falls under the category of biosimilar drugs, specifically a biosimilar to trastuzumab. Trastuzumab is a monoclonal antibody that is commonly used in the treatment of HER2-positive breast cancer. Kanjinti works by targeting the HER2 protein, which is overexpressed in some breast cancers, and inhibiting its growth.

As a medical professional, it is important to understand the role of biosimilar drugs like Kanjinti in the treatment of cancer. Biosimilars are highly similar to their reference biologic drugs, but may have minor differences in their chemical structure. These differences do not affect the safety or efficacy of the drug, but they may impact factors such as immunogenicity or dosing.

Kanjinti has been approved by the FDA as a biosimilar to trastuzumab, meaning that it has been shown to have similar efficacy and safety profiles to the reference drug. This provides an additional treatment option for patients with HER2-positive breast cancer, potentially increasing access to this life-saving therapy.

It is important to discuss the use of Kanjinti with your patients, explaining the benefits and potential side effects of the medication. As with any cancer treatment, close monitoring and communication with patients is essential to ensure the best possible outcomes.

In conclusion, Kanjinti is a valuable addition to the treatment options available for patients with HER2-positive breast cancer. As a medical professional, it is important to stay informed about biosimilar drugs like Kanjinti and to discuss their use with patients in a clear and compassionate manner.

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The information provided on RxDB.net is for informational purposes only and is not intended to replace professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare professional, such as a doctor or pharmacist, for any questions or concerns regarding your health, medications, or medical conditions. Reliance on any information provided on this website is solely at your own risk. RxDB.net does not provide medical or pharmaceutical services and is not liable for any decisions made based on the information contained herein.

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