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Sanofi Receives FDA Approval of Soliqua™ 100/33 for the Treatment of Adults with Type 2 Diabetes – PARIS, Nov. 21, 2016 /PRNewswire-USNewswire/ — Sanofi announced today that the U.S. Food and Drug Administration (FDA) approved once-daily Soliqua™ 100/33 (insulin glargine & lixisenatide injection) 100 Units/mL & 33 mcg/mL for the …

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“Soliqua 100/33 is an alternate approach that can help adults living with type 2 diabetes uncontrolled on basal insulin or lixisenatide to reach their treatment goal,” said Elias Zerhouni, …

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Sanofi SNY announced that the FDA has approved its once-daily injection, Soliqua 100/33 – a combination of its diabetes drugs, Lantus and lixisenatide (EU trade name: Lyxumia) for the treatment of type 2 diabetes in adults who have …