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trastuzumab emtansine (Kadcyla®)

 

Status: Excluded due to NICE appraisal

Product meets AWMSG exclusion criteria due to NICE appraisal TA458: Trastuzumab emtansine for treating HER2-positive advanced breast cancer after trastuzumab and a taxane (replaced TA371)

Medicine details

Medicine name trastuzumab emtansine (Kadcyla®)
Formulation 100 mg, 160 mg powder for concentrate for solution for infusion
Reference number 1390
Indication

As a single agent, for the treatment of adult patients with HER2-positive, unresectable locally advanced or metastatic breast cancer who previously received trastuzumab and a taxane, separately or in combination. Patients should have either received prior therapy for locally advanced or metastatic disease, or developed disease recurrence during or within six months of completing adjuvant therapy

Company Roche Products Ltd
BNF chapter Malignant disease & immunosuppression
Assessment type N/A
Status Excluded due to NICE appraisal
Date of issue 26/02/2014
NICE guidance

TA458: Trastuzumab emtansine for treating HER2-positive advanced breast cancer after trastuzumab and a taxane (replaced TA371)

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