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Kanjinti

Generic name: trastuzumabtras-TOO-zoo-mab ]
Brand names: Herceptin, Herzuma, Kanjinti, Ogivri, Ontruzant, Trazimera
Drug class: HER2 inhibitors

Medically reviewed by Drugs.com on Mar 26, 2024. Written by Cerner Multum.

What is Kanjinti?

Kanjinti is used to treat certain types of breast cancer or stomach cancer, sometimes in combination with other cancer medicines.

Kanjinti is sometimes used when the cancer has spread to other parts of the body (metastatic).

Kanjinti may also be used for purposes not listed in this medication guide.

Kanjinti side effects

Get emergency medical help if you have signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat.

Some side effects may occur during the injection, or in the days afterward. Tell your caregiver right away if you feel dizzy, nauseated, itchy, light-headed, weak, short of breath, or if you have a headache, fever, chills, or chest pain.

Kanjinti may cause serious side effects. Call your doctor at once if you have:

Your cancer treatments may be delayed or permanently discontinued if you have certain side effects.

Common side effects of Kanjinti may include:

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

Warnings

Do not use if you are pregnant. Use effective birth control, and tell your doctor if you become pregnant during treatment.

Kanjinti can cause heart failure, especially if you have heart disease or if you are also receiving certain other cancer medicines.

Some side effects may occur during the injection. Tell your caregivers if you feel dizzy, nauseated, light-headed, weak, short of breath, or if you have a headache, fever, or chills.

Before taking this medicine

Tell your doctor if you have ever had:

Kanjinti can cause heart failure, especially if you have heart disease or if you are also receiving certain other cancer medicines (such as daunorubicin, doxorubicin, epirubicin, or idarubicin).

You may need to have a negative pregnancy test before starting this treatment.

Do not use Kanjinti if you are pregnant. Kanjinti can cause injury or death to the unborn baby. Use effective birth control to prevent pregnancy while you are using this medicine and for at least 7 months after your last dose. Tell your doctor if you become pregnant.

If you become pregnant while using Kanjinti or within 7 months after you stop, your name may be listed on a pregnancy registry to track the effects of trastuzumab on the baby.

It may not be safe to breastfeed while using this medicine and for up to 7 months after your last dose. Ask your doctor about any risk.

How is Kanjinti given?

Your doctor will perform a medical test to make sure Kanjinti is the right medicine to treat your cancer.

Kanjinti is given as an infusion into a vein. A healthcare provider will give you this injection.

Kanjinti is usually given once every week or every 1 to 3 weeks. Follow your doctor's dosing instructions very carefully.

This medicine must be given slowly, and the infusion can take up to 90 minutes to complete.

You may need frequent medical tests to be sure this medicine is not causing harmful effects. Your cancer treatments may be delayed based on the results.

Your heart function may need to be checked before and during treatment with Kanjinti. You may also need heart function testing every 6 months for 2 years after your last dose of this medicine.

Kanjinti is usually given for 52 weeks, or until your body no longer responds to the medication.

Kisqali, Verzenio, Trodelvy, tamoxifen, letrozole, Keytruda, Arimidex, pembrolizumab, capecitabine, paclitaxel

What happens if I miss a dose?

Call your doctor for instructions if you miss an appointment for your Kanjinti.

What happens if I overdose?

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

What should I avoid while receiving Kanjinti?

Follow your doctor's instructions about any restrictions on food, beverages, or activity.

What other drugs will affect Kanjinti?

Other drugs may affect Kanjinti, including prescription and over-the-counter medicines, vitamins, and herbal products. Tell your doctor about all your current medicines and any medicine you start or stop using.

Kanjinti can have long lasting effects on your heart, especially if you receive other cancer medicines. For at least 7 months after your last dose of trastuzumab, tell any doctor who treats you that you have used Kanjinti.

Does Kanjinti interact with my other drugs?

Enter other medications to view a detailed interaction report.

Kanjinti Biosimilars

Biosimilar and interchangeable products are biological products that are highly similar to and have no clinically meaningful differences from the reference product.

Reference products

These are biological products that have already been approved by the FDA, against which biosimilar products are compared. There is 1 for Kanjinti.

Herceptin (trastuzumab) - Genentech, Inc.
Formulation type Strength
Multi-Dose Vial 420 mg Discontinued
Single-Dose Vial 150 mg

View Herceptin information in detail.

Herceptin biosimilar products

Biosimilar products can only be dispensed in place of the reference product if the healthcare provider specifically prescribes the biosimilar product by name.

Pharmacy laws for biosimilar prescribing may vary by state

Herzuma (trastuzumab-pkrb) - CELLTRION, Inc.
Formulation type Strength
Multi-Dose Vial 420 mg
Single-Dose Vial 150 mg

View Herzuma information in detail.

Kanjinti (trastuzumab-anns) - Amgen Inc.
Formulation type Strength
Multi-Dose Vial 420 mg
Single-Dose Vial 150 mg
Ogivri (trastuzumab-dkst) - Biocon Biologics Inc.
Formulation type Strength
Multi-Dose Vial 420 mg
Single-Dose Vial 150 mg

View Ogivri information in detail.

Ontruzant (trastuzumab-dttb) - Samsung Bioepis Co., Ltd.
Formulation type Strength
Multi-Dose Vial 420 mg
Single-Dose Vial 150 mg

View Ontruzant information in detail.

Trazimera (trastuzumab-qyyp) - Pfizer Ireland Pharmaceuticals
Formulation type Strength
Multi-Dose Vial 150 mg
Multi-Dose Vial 420 mg

View Trazimera information in detail.

Popular FAQ

What are biosimilar drugs and how do they compare to biologics?

A biosimilar is a biological product that is similar to a reference biologic (usually the originally approved product) and for which there are no clinically meaningful differences in terms of safety, purity, and potency. One example is Amjevita (adalimumab-atto), the first biosimilar approved for Humira (adalimumab) in 2016. Continue reading

What are the biosimilars of Herceptin?

The biosimilars of Herceptin are Herzuma, Kanjinti, Ogivri, Ontruzant and Trazimera Continue reading

How long can you stay on Herceptin and Perjeta?

If you are receiving Perjeta for treatment of HER2+ early breast cancer, you may continue treatments with Herceptin every 3 weeks for one year (18 cycles total). For the treatment of HER2+ metastatic breast cancer, you will receive Perjeta and Herceptin until the medicine no longer controls your breast cancer or you have side effects that require you to stop treatment. You may receive other treatments with these medications. Continue reading

What happens after Herceptin treatment?

After Herceptin treatment, your doctor will monitor you regularly for cancer progression, advise you not to become pregnant for at least 7 months (if you are of childbearing potential), and test your heart every 6 months for at least 2 years, because there is a higher risk of developing long-term heart damage in people who take Herceptin. Continue reading

How long can I stay on Herceptin?

Treatment regimens for Herceptin vary depending on hospital protocols, but for the treatment of HER2+ early breast cancer, treatment is usually continued for one year (up to 18 cycles). Continue reading

What is TDM1 chemotherapy?

T-DM1 chemotherapy refers to treatment with Kadcyla, which is a targeted treatment that may be used to treat HER2-positive breast cancer in women who meet certain criteria. The chemical name for Kadcyla is T-DM1 (also called ado-trastuzumab emtansine) and it is a combination of two medicines: trastuzumab which is a targeted treatment and DM1 which is a cytotoxic agent (also known as mertansine). Trastuzumab targets HER2-expressing breast cancer cells and delivers DM1 directly to them. Continue reading

More FAQ

Further information

Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed.

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.