Blockchain startup R3 cuts fund-raising target to $150 million: source
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Sanofi's (SNY) Soliqua 100/33 Approved by FDA as T2D Treatment
November 22, 2016 6:14 AM ESTSanofi (NYSE: SNY) announced 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 treatment of adults with type 2 diabetes inadequately controlled on basal insulin (less than 60 Units daily) or lixisenatide*.
Soliqua 100/33 is the combination of Lantus® (insulin glargine 100 Units/mL) and lixisenatide, a GLP-1 receptor agonist, in a once-daily injection, studied in a Phase 3 program of more than 1,900 patients. In an insulin intensification study, Soliqua... More
