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This website contains promotional content and is intended for Healthcare Professionals based in the United Kingdom only. Some content may only be relevant to HCPs practising in Great Britain (England, Scotland and Wales) according to product availability. This website is optimised for desktop use, and some features may perform differently on mobile devices.

Adverse event reporting can be found at the bottom of the page.

Prescribing Information for SARCLISA® (isatuximab) can be found via the Product Card at the bottom of the page.

Dr Sally Moore Consultant Haematologist, Royal United Hospital, Bath and University Hospital, Bristol

Dr Sally Moore talks through treatment options for a 73-year-old female patient with transplant-ineligible newly diagnosed multiple myeloma who is being considered for 
SARCLISA® (isatuximab) + VRd treatment.

Get in touch with the Oncology Team

Sarclisa logo

Ti NDMM

Learn more  →

Prescribing information UK

MAT-XU-2202578 (v7.0)
Date of preparation: August 2025  

MAT-XU-2600376 (v1.0) Date of Preparation: February 2026  


Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. Adverse events should also be reported to the Sanofi drug safety department on Tel: +44 (0) 800 0902 314. Alternatively, send via email to UK-drugsafety@sanofi.com