
The US Food and Drug Administration (FDA) has granted accelerated approval to French pharma major Sanofi’s (Euronext: SAN) Tzield (teplizumab-mzwv) to delay the decline in endogenous (own) insulin production in children aged eight to 17 years recently diagnosed with stage 3 type 1 diabetes (T1D).
The company noted that Tzield is not effective as a disease-modifying therapy in non-autoimmune dysglycemic conditions.
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Chairman, Sanofi Aventis UK
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