এই পেইজের তথ্য মেডিকেল পরামর্শ হিসাবে বিবেচিত নয় এবং কোন চিকিৎসকের সাথে পরামর্শ করার বিকল্প হিসাবেও ব্যবহার করা যাবেনা ।
Kadcyla is an Antibody Drug Conjugate (ADC), which combines the HER2-targeting properties of Herceptin (trastuzumab) and the cytotoxic chemotherapy agent DM1. In Kadcyla, trastuzumab and DM1 are joined together using a ‘stable linker’ to deliver DM1 directly to HER2-positive cancer cells.1
Kadcyla is approved as a single agent in the US, EU and many other countries for the treatment of people with HER2-positive advanced breast cancer who previously received Herceptin and taxane chemotherapy, separately or in combination.1
In Bangladesh Kadcyla is approved for the following indications.2
Kadcyla, as a single agent, is indicated for the treatment of patients with HER2-positive, unresectable locally advanced or metastatic breast cancer who have received prior treatment with trastuzumab and a taxane.
Kadcyla, as a single agent, is indicated for the adjuvant treatment adult of patients with HER2-positive early breast cancer who have residual disease, breast and/or lymph nodes after pre-operative systemic treatment that included HER2 targeted therapy.
For more disease and medicine related queries you may discuss with your physician.
In Bangladesh Kadcyla is available as
Vials 100 mg
Vials 160 mg
Are a woman who could become pregnant, or may be pregnant
If a patient becomes pregnant while receiving Kadcyla, or within 7 months following the last dose of Kadcyla, please immediately report pregnancy to the local RocheAdverse Event Line at
Additional information will be requested during a Kadcyla-exposed pregnancy and the first year of the infant’s life. This will enable Roche to better understand the safety of Kadcyla and to provide appropriate information to health authorities, healthcare providers, and patients
For additional information, please refer to
রোগীর সুরক্ষা এবং ঔষধের গুণগত মান নিশ্চিত করার জন্য, আমরা জোরালোভাবে পরামর্শ দিয়ে থাকি যে, কেনার আগে অবশ্যই ভালভাবে দেখে নেবেন যে প্রতিটি ঔষধে Roche Hologram Sticker, আছে কিনা এবং DGDA অনুমোদিত DAR (Drug Administration Registration) Number আছে কিনা। অন্য কোন উৎস থেকে প্রাপ্ত ঔষধ এর দায় রেডিয়েন্ট বা রোশ বাংলাদেশ এর কেউই গ্রহণ করবে না।