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Want to know more about BLENREP (belantamab mafodotin)?

Get in touch with your local GSK Ireland Team today to learn more.

Adverse event reporting information can be found at the bottom of this page

Hazel Melia

Haematology Medical Advisor

hazel.x.melia@gsk.com

GET IN TOUCH

Ailbhe O'Toole

Haematology Brand Lead

ailbhe.x.o'toole@gsk.com

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Leigh Lehane

Medical Science Liaison Haematology

leigh.a.lehane@gsk.com

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Muireann Nyhan

Key Account Manager Haematology

Muireann.e.nyhan@gsk.com

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Summary of product characteristics & Patient information leaflet for Blenrep 70mg/100mg powder for concentrate for solution for infusion

open

INDICATION

Blenrep is indicated in adults for the treatment of relapsed or refractory multiple myeloma:

in combination with bortezomib and dexamethasone in patients who have received at least one prior therapy; and
in combination with pomalidomide and dexamethasone in patients who have received at least one prior therapy including lenalidomide.

Reference

BLENREP. Summary of Product Characteristics. GlaxoSmithKline. 2026.

Adverse events should be reported directly to the Health Products Regulatory Authority (HPRA) on their website: www.hpra.ie. Adverse events should also be reported to GlaxoSmithKline on 1800 244 255 or via the online form gsk.public.reportum.com

▼This medicine is subject to additional monitoring. This will allow quick identification of new safety information.

BLENREP is a registered trademark of the GlaxoSmithKline group of companies.

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Registered in Ireland: GlaxoSmithKline (Ireland) Limited, a private company limited by shares, and a member of the GlaxoSmithKline group of companies. Registered in Ireland with Company Number 15513.
Registered office: 12 Riverwalk, Citywest Business Campus, Dublin 24, Ireland.

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