Lixisenatide in the treatment of type 2 diabetes genetic,diabetes mellitus pdf ada 2015 diabetes,diabetic diet plan snacks uk,s-works roubaix vs tarmac - Plans On 2016

In March 2013, Lyxumia® was launched in the first markets by Sanofi, who holds global development and commercial rights to the product under a license agreement with Zealand. Adding a GLP-1 agonist with pronounced effect on PPG complements basal insulin  in normalizing blood sugar levels over the course of the day. Lyxumia®(lixisenatide) is associated with a significant lowering of HbA1C (glycosylated hemoglobin), a beneficial effect on body weight and a predominant effect on lowering meal related glucose (post-prandial glucose, PPG). In February 2013, FDA accepted a New Drug Application (NDA) filed by Sanofi for lixisenatide in the US. The decision to withdraw the lixisenatide application followed discussions with the FDA regarding its proposed process for the review of interim data.


The evaluation of lixisenatide in acute coronary syndrome (ELIXA) study is an eventdriven cardiovascular (CV) outcome study in Type 2 diabetic patients with high CV risk. The fixed-ratio combination has been evaluated by Sanofi in a Phase IIb study versus Lantus® alone for its effect on glycemic control, as measured by HbA1c reduction over 24 weeks, in 323 Type 2 diabetic patients treated with metformin. This website uses cookies to gather statisticts and in order to improve your user experience.
Lixisenatide works by controlling blood sugar by increasing the production of insulin which results in slowing down the body's absorption of sugar. Sanofi believes that potential public disclosure of early interim data, even with safeguards, could potentially compromise the integrity of the ongoing ELIXA study.


As of August, 2013, the study was fully enrolled and study completion is expected in 2015, with results available that same year.



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