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

This is intended for HCPs practising in Great Britain (England, Scotland, Wales) only.

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

In this video, you'll learn about

An independent UK real world study presented by Professor Basu and Dr Ramasamy. This data was generated across 24 centres including 107 patients, and demonstrated that SARCLISA® + Pd is effective and achievable in routine clinical care with outcomes comparable to those seen in the phase 3 ICARIA-MM trial.1,2

Overview of SARCLISA®


Find out more about SARCLISA® + Pd efficacy and safety data and dosing information.

Dosing and Administration Guide


Download a handy guide to SARCLISA dosing and administration information

Patient Booklet


Download SARCLISA® patient information.

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Overview of SARCLISA®


Find out more about SARCLISA® + Pd efficacy and safety data and dosing information.

Dosing and Administration Guide


Download a handy guide to SARCLISA dosing and administration information

Patient Booklet


Download SARCLISA® patient information.

Get in touch with the Oncology Team

Relapsed Refractory Multiple Myeloma Product

Sarclisa logo GB only

MAT-XU-2202578 (v4.0)
Date of preparation: June 2024

▼This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions.

References
  1. Attal M, et alLancet. 2019;394:2096–107.

  2. Djebbari F, et alHemasphere. 2022;6(6):e738.

MAT-XU-2202566 (v3.0) Date of Preparation: June 2024