פרטים כלליים
שם
Name
קנג'ינטי 150 מ"ג
KANJINTI 150 MG
יצרן
AMGEN EUROPE B.V., NETHERLANDS
בעל רישום
AMGEN EUROPE B.V.
שימוש
צורת מינון
Dosage Form
אבקה להכנת תמיסה מרוכזת לעירוי
POWDER FOR CONCENTRATE FOR SOLUTION FOR INFUSION
דרך מתן
Usage Form
תוך-ורידי
I.V
תמונה חסרה
מחירים לצרכן
לא נמצא מידע
חומר פעיל
חומר פעיל
כמות
150 MG/VIAL
תרופות אחרות בעלות אותם מרכיבים
ATC
עלונים
עדכון רישום
סוג עדכון
תאריך עדכון
27.01.2022
27.01.2022
08.07.2021
08.07.2021
08.11.2020
08.11.2020
08.11.2020
08.11.2020
11.05.2020
11.05.2020
התוויה מאושרת
Metastatic breast cancer (MBC)KANJINTI is indicated for the treatment of patients with metastatic breast cancer who have tumors that overexpress HER2;1. As a single agent, for the treatment of those patients who have received one or more chemotherapy regimens for their metastatic disease.2. In combination with Paclitaxel or Docetaxel 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 patient with hormone-receptor positive metastatic breast cancer.Early breast cancer (EBC)KANJINTI is indicated to treat patients with HER2 positive early breast cancer following surgery and chemotherapy (neoadjuvant or adjuvant) either alone or in combination with chemotherapy excluding anthracyclines.Kanjinti should only be used in patients whose tumors have either HER2 overexpression or HER2 gene amplification as determined by an accurate and validated assay.HER2 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 gastroesophageal junction who have not received prior anti-cancer treatment for their metastatic disease.KANJINTI should only be used in patients with metastatic gastric cancer (MGC) whose tumours have HER2 overexpression as defined by IHC 2+ and a confirmatory FISH+ result, or IHC 3+, as determined by an accurate and validated assay.
בסל הבריאות
כן
מספר רישום
164-56-36111-00
תנאי ניפוק
תרופה במרשם
מגבלות
ללא הגבלות