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BLENREP is indicated in adults for the treatment of multiple myeloma:1
- 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
Belantamab mafodotin with bortezomib and dexamethasone for treating relapsed or refractory multiple myeloma after 1 or more treatments [ID6212]
Read the draft guidance from NICE for BLENREP in combination with bortezomib and dexamethasone.
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Belantamab mafodotin with pomalidomide and dexamethasone for previously treated multiple myeloma [ID6211]
Read the draft guidance from NICE for BLENREP in combination with pomalidomide and dexamethasone.
By clicking this link, you will leave GSKPro.com, a website provided by GSK. This link will take you to a website which our Privacy Statement, Cookie Statement and Terms of Use Agreement do not apply. GSK does not endorse and/or influence the content found on websites not owned/operated by GSK.
Abbreviations
2L, second line; NICE, National Institute for Health and Care Excellence; SMC, Scottish Medicines Consortium.
References
- BLENREP. Summary of Product Characteristics. GlaxoSmithKline. 2026.
- NICE. ID6212. Available at https://www.nice.org.uk/guidance/indevelopment/gid-ta11203. Accessed February 2026.
- NICE. ID6211. Available at: https://www.nice.org.uk/guidance/indevelopment/gid-ta11201. Accessed February 2026.
- SMC. SMC2727. Available at https://scottishmedicines.org.uk/medicines-advice/belantamab-mafodotin-blenrep-full-smc2727/. Accessed February 2026.
▼This product is subject to additional monitoring. Adverse events should be reported. Reporting forms and information can be found at yellowcard.mhra.gov.uk or via the Yellow Card app (available on the Apple App Store or Google Play Store). Adverse events should also be reported to GlaxoSmithKline on 0800 221 441 or UKSafety@GSK.com.
February 2026 | PM-GB-BLM-WCNT-250040 (V1.0)
