Sanofi wins EU approval for Teizeild to delay onset of stage 3 type 1 diabetes

Reuters01-12

<a href="https://laohu8.com/S/GCVRZ">Sanofi</a> wins EU approval for Teizeild to delay onset of stage 3 type 1 diabetes

Sanofi SA has received approval from the European Commission for Teizeild (teplizumab) to delay the onset of stage 3 type 1 diabetes (T1D) in adults and children aged eight years and older with stage 2 T1D. The approval follows a positive opinion from the European Medicines Agency's Committee for Medicinal Products for Human Use and is based on results from the TN-10 phase 2 study, which demonstrated that Teizeild delayed the onset of stage 3 T1D by a median of two years compared to placebo. Teizeild is the first disease-modifying therapy for T1D approved in the EU. The therapy is also approved in the US, UK, China, Canada, Israel, Saudi Arabia, United Arab Emirates, and Kuwait for similar indications. Regulatory reviews in other regions are ongoing.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Sanofi SA published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW1001158645-en) on January 12, 2026, and is solely responsible for the information contained therein.

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The approval follows a positive opinion from the European Medicines Agency's Committee for Medicinal Products for Human Use and is based on results from the TN-10 phase 2 study, which demonstrated that Teizeild delayed the onset of stage 3 T1D by a median of two years compared to placebo. Teizeild is the first disease-modifying therapy for T1D approved in the EU. The therapy is also approved in the US, UK, China, Canada, Israel, Saudi Arabia, United Arab Emirates, and Kuwait for similar indications. Regulatory reviews in other regions are ongoing.\n      \n\n\nDisclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Sanofi SA published the original content used to generate this news brief via GlobeNewswire (Ref. 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