- Approval Id
- d60e399392164dad
- Drug Name
- KANJINTI POWDER FOR INJECTION 440 MG/VIAL
- Product Name
- KANJINTI POWDER FOR INJECTION 440 MG/VIAL
- Approval Number
- SIN16207P
- Approval Date
- 2021-05-25
- Registrant
- AMGEN BIOTECHNOLOGY SINGAPORE PTE LTD
- Licence Holder
- AMGEN BIOTECHNOLOGY SINGAPORE PTE LTD
- Drug Type
- Therapeutic
- Forensic Classification
- Prescription Only
- Dosage Form
- INJECTION, POWDER, FOR SOLUTION
- Dosage
- **2.2 Dosage and Administration**
**General**
HER2 testing is mandatory prior to initiation of KANJINTI therapy.
Substitution by any other biological medicinal product requires the consent of the prescribing physician.
The safety and efficacy of alternating or switching between Herceptin and products that are biosimilar but not deemed interchangeable to Herceptin has not been established. Therefore, the benefit/risk of alternating or switching need to be carefully considered.
KANJINTI should be administered by a qualified health care professional.
In order to prevent medication errors, it is important to check the vial labels to ensure that the drug being prepared and administered is KANJINTI (trastuzumab) and not trastuzumab emtansine.
_**KANJINTI IV (see section 4. Pharmaceutical Particulars** – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information **):**_
KANJINTI IV is not to be used for subcutaneous administration and should be administered as intravenous infusion.
Do not administer as an intravenous push or bolus.
**Metastatic Breast Cancer**
_Weekly schedule:_
_Loading dose:_ The recommended initial loading dose is 4 mg/kg body weight KANJINTI IV administered as a 90-minute intravenous infusion. Patients should be observed for fever and chills or other infusion-associated symptoms (see 2.6 Undesirable effects – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). Interruption of the infusion may help control such symptoms. The infusion may be resumed when symptoms abate.
_Subsequent doses:_ The recommended weekly dose of KANJINTI IV is 2 mg/kg body weight. If the prior dose was well tolerated, the dose can be administered as a 30-minute infusion. Patients should be observed for fever and chills or other infusion-associated symptoms (see 2.6 Undesirable effects – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_).
_Administration in combination with an aromatase inhibitor_
In the pivotal trial trastuzumab IV and anastrozole were administered from day 1. There were no restrictions on the relative timing of trastuzumab IV and anastrozole at administration (for dose, see the Product Information for anastrozole or other aromatase inhibitors).
_3-weekly schedule:_
Alternatively, the following loading and subsequent doses are recommended for monotherapy and in combination with paclitaxel or an aromatase inhibitor.
Initial KANJINTI IV loading dose of 8 mg/kg body weight, followed by 6 mg/kg body weight 3 weeks later and then 6 mg/kg repeated at 3-weekly intervals administered as infusions over approximately 90 minutes. If the initial loading dose was well tolerated, the subsequent doses can be administered as a 30-minute infusion.
**Early Breast Cancer**
_3-weekly schedule:_
As a three-weekly regimen the recommended initial loading dose of KANJINTI IV is 8 mg/kg body weight. The recommended maintenance dose of KANJINTI at three-weekly intervals is 6 mg/kg body weight, beginning three weeks after the loading dose.
_Alternative weekly schedule:_
As a weekly regimen (initial loading dose of 4 mg/kg followed by 2 mg/kg every week) concomitantly with paclitaxel following chemotherapy with doxorubicin and cyclophosphamide.
**Metastatic Gastric Cancer**
_3-weekly schedule:_
KANJINTI IV is administered at an initial loading dose of 8 mg/kg body weight, followed by 6 mg/kg body weight 3 weeks later and then 6 mg/kg repeated at 3-weekly intervals administered as infusions over approximately 90 minutes. If the initial loading dose is well tolerated, the subsequent doses can be administered as a 30-minute infusion (see section 3.1 for chemotherapy combination dosing – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_).
**Duration of Treatment**
In clinical studies, patients with metastatic breast cancer or metastatic gastric cancer were treated with trastuzumab until progression of disease or unmanageable toxicity. Patients with early breast cancer should be treated for 1 year or until disease recurrence or unmanageable toxicity, whichever occurs first. Extending treatment in EBC beyond one year is not recommended (see section 3.1.2 Clinical / Efficacy Studies – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_).
For instructions for use and handling refer to Section 4.6 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_.
**Dose Modification**
If the patient develops an infusion-related reaction (IRR), the infusion rate of KANJINTI IV may be slowed or interrupted (see section 2.4 Warnings and Precautions – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_).
No reductions in the dose of KANJINTI were made during clinical trials. Patients may continue KANJINTI therapy during periods of reversible, chemotherapy-induced myelosuppression, but they should be monitored carefully for complications of neutropenia during this time. The specific instructions to reduce or hold the dose of chemotherapy should be followed.
**Missed Doses**
If the patient has missed a dose of KANJINTI IV by one week or less, then the usual maintenance dose (weekly regimen: 2 mg/kg; three-weekly regimen: 6 mg/kg) should be administered as soon as possible. Do not wait until the next planned cycle. Subsequent KANJINTI IV maintenance doses be administered 7 days or 21 days later according to the weekly or three-weekly schedules, respectively.
If the patient has missed a dose of KANJINTI IV by more than one week, a re-loading dose of KANJINTI IV should be administered over approximately 90 minutes (weekly regimen: 4 mg/kg; 3-weekly regimen: 8 mg/kg) as soon as possible. Subsequent KANJINTI IV maintenance doses (weekly regimen: 2 mg/kg; three-weekly regimen 6 mg/kg respectively) should be administered 7 days or 21 days later according to the weekly or three-weekly schedules respectively.
**2.2.1 Special Dosage Instructions**
_Geriatric use_
Data suggest that the disposition of KANJINTI is not altered based on age or serum creatinine (see Pharmacokinetics in Special Populations – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). In clinical trials, patients ≥ 65 years of age did not receive reduced doses of KANJINTI. Dedicated pharmacokinetic studies in the elderly and those with renal or hepatic impairment have not been carried out. However in a population pharmacokinetic analysis, age and renal impairment were not shown to affect KANJINTI disposition.
_Paediatric use_
The safety and efficacy of KANJINTI in pediatric patients < 18 years of age have not been established.
- Route Of Administration
- INTRAVENOUS
- Indication Info
- **2.1 Therapeutic Indications**
_**KANJINTI IV**_
_Metastatic Breast Cancer (MBC)_
KANJINTI is indicated for the treatment of patients with metastatic breast cancer who have tumors that overexpress HER2:
1. as monotherapy for the treatment of those patients who have received one or more chemotherapy regimens for their metastatic disease
2. in combination with paclitaxel for the treatment of those patients who have not received chemotherapy for their metastatic disease
3. in combination with an aromatase inhibitor for the treatment of postmenopausal patients with hormone-receptor positive metastatic breast cancer, not previously treated with KANJINTI. This indication is based on data from one Phase III trial which studied the use of KANJINTI in combination with anastrozole (see 3.1.2 Clinical / Efficacy Studies – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_).
Experience with other aromatase inhibitors is limited.
_Early Breast Cancer (EBC)_
KANJINTI is indicated for the treatment of patients with HER2 positive early breast cancer.
- following surgery, chemotherapy (neoadjuvant or adjuvant) and radiotherapy (if applicable) (see section 3.1 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_).
- following adjuvant chemotherapy with doxorubicin and cyclophosphamide, in combination with paclitaxel or docetaxel.
- in combination with adjuvant chemotherapy consisting of docetaxel and carboplatin.
- in combination with neoadjuvant chemotherapy followed by adjuvant KANJINTI therapy, for locally advanced (including inflammatory) disease or tumours > 2 cm in diameter (see sections 2.4 and 3.1 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_).
KANJINTI should only be used in patients whose tumours have either HER2 overexpression or HER2 gene amplification as determined by an accurate and validated assay.
_Metastatic Gastric Cancer (MGC)_
KANJINTI in combination with capecitabine or 5-fluorouracil and cisplatin is indicated for the treatment of patients with HER2 positive metastatic adenocarcinoma of the stomach or gastro-esophageal junction who have not received prior anti-cancer treatment for their metastatic disease.
KANJINTI should only be used in patients with metastatic gastric cancer whose tumours have HER2 overexpression as defined by IHC2+ and a confirmatory FISH+ result, or IHC3+, as determined by an accurate and validated assay.
- Contraindications
- **2.3 Contraindications**
Patients with known hypersensitivity to trastuzumab, murine proteins, hyaluronidase or to any other component of the product. Patients with severe dyspnoea at rest due to complications of advanced malignancy or requiring supplementary oxygen therapy.
- Atc Code
- L01XC03
- Atc Item Name
- xl 01 xc 03
- Pharma Manufacturer Name
- AMGEN BIOTECHNOLOGY SINGAPORE PTE. LTD.
- Company Detail Path
- /organization/2674a0bc2a636200/amgen-biotechnology-singapore-pte-ltd
