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ibrutinib (Imbruvica®)

 

Status: Superseded

AWMSG ADVICE SUPERSEDED BY NICE GUIDANCE ISSUED JANUARY 2017. Refer to TA429: Ibrutinib for previously treated chronic lymphocytic leukaemia and untreated chronic lymphocytic leukaemia with 17p deletion or TP53 mutation for full guidance on NICE recommendations, including any specific restrictions on the use of the technology. AWMSG documentation provided for reference only.

 Statement of Advice (SOA): ibrutinib (Imbruvica) 2027 (PDF, 102Kb)

Medicine details

Medicine name ibrutinib (Imbruvica®)
Formulation 140 mg hard capsule
Reference number 2027
Indication

Treatment of adult patients with chronic lymphocytic leukaemia (CLL) who have received at least one prior therapy, or in first line in the presence of 17p deletion or TP53 mutation in patients unsuitable for chemo-immunotherapy

Company Janssen-Cilag Ltd
BNF chapter Malignant disease & immunosuppression
Submission type Non-submission
Status Superseded
Ratification by Welsh Government 10/06/2016
Date of issue 15/06/2016
NICE guidance

TA429: Ibrutinib for previously treated chronic lymphocytic leukaemia and untreated chronic lymphocytic leukaemia with 17p deletion or TP53 mutation

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