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

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TZIELD (teplizumab) can give patients more symptom-free time in Stage 2 autoimmune T1D vs placebo, delaying a lifetime of symptom management and insulin therapy1–3

A delay in the onset of stage 3 T1D may provide your patients with:

More insulin-free years4-6

Delaying the social stigma and lifestyle disruptions that come with managing T1D4,5,7

Time for vigilant monitoring of signs and symptoms of DKA6

To reduce the risk of hospitalisation with DKA6

Increased opportunities to learn about glycaemic control8

So your patients can learn how to properly manage their disease9

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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.4

T1D, Type 1 diabetes.

  1. Sims EK, et al. Sci Transl Med. 2021; 13(583): eabc8980.
  2. Insel RA, et al. Diabetes Care. 2015; 38(10): 1964–1974.
  3. Lledó-Delgado A, et al. J Clin Invest. 2024; 134(18): e177492.
  4. TZIELD® (teplizumab) UK Summary of Product Characteristics.
  5. Edelman S. J Fam Pract. 2023; 72(6 Suppl): S19-S24.
  6. Ayers AT, et al. J Diabetes Sci Technol. 2025; 19(6): 1441-1447.
  7. Ashraf MN and Cheng AYY. Diabetes Ther. 2024; 15(2): 311-316.
  8. Phillip M, et al. Diabetes Care. 2024; 47(8): 1276-1298.
  9. American Diabetes Association Professional Practice Committee. Diabetes Care. 2022; 45(Suppl 1): S83-S96.

MAT-XU-2500772 (v2.0) | June 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