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

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Support for hcps

For HCPs


We're here to support you with useful resources about Tzield, Early Detection and to prepare you and your team for the first Tzield infusion.

Infusion Readiness Tools

Dosing Calculator

Want an easy way to calculate the TZIELD dosing regimen? This dosing calculator helps you to quickly and accurately determine doses for your patients. A practical resource to share with colleagues and your MDT unit during TZIELD infusions.

Calculate dosing regimen
BSA Calculator

Educational material

Peer Perspectives

What are your peers saying?

Hear from Professor Parth Narendran, Dr Renuka Dias, Dr Theodora Papanikolau and Jenny Cooper, who are sharing their experience with Teplizumab.

INDICATION: TZIELD is indicated to delay the onset of Stage 3 T1D in adult and paediatric patients 8 years of age and older with  Stage 2 T1D.1

MDT, multi-disciplinary team; T1D, Type 1 diabetes.

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INDICATION: TZIELD is indicated to delay the onset of Stage 3 T1D in adult and paediatric patients 8 years of age and older with  Stage 2 T1D.1

ABCD, Association of British Clinical Diabetologists; BSPED, British Society for Paediatric Endocrinology and Diabetes; ISPAD, International Society for Pediatric and Adolescent Diabetes; MDT, multi-disciplinary team; T1D, Type 1 diabetes.

  1. TZIELD® (teplizumab) UK Summary of Product Characteristics. 2025.

MAT-XU-2600465 (v1.0) | March 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