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This article originally posted 15 December, 2011 and appeared in  MedicationType 2 DiabetesGLP-1 AgonistIssue 604

GLP-1 Lixisenatide Phase III Results

Adding lixisenatide to metformin and insulin glargine significantly reduced glycated hemoglobin levels and improved post-prandial glucose in patients with type 2 diabetes....

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In the randomized, double-blind, placebo-controlled GetGoal Duo 1 study, patients uncontrolled on oral medication -- mainly metformin -- received either lixisenatide once-daily or placebo while insulin glargine and metformin were continued. Patients had already decreased their HbA1c -- the primary efficacy endpoint -- on average from 8.60% to 7.60% during a 12-week run-in period with insulin glargine.

After a 24-week randomization phase, those on lixisenatide had further significantly decreased HbA1c compared with placebo (P<0.0001) to a mean value of 6.96%, with a significantly higher percentage of patients achieving target HbA1c less than 7.0% with lixisenatide compared with placebo (56.3% versus 38.5%, respectively, P=0.0001), according to Sanofi's press release.

Sanofi has submitted a request to the European Medicines Agency for regulatory approval and expects to submit a similar request to the FDA toward the end of 2012.

The full study results from GetGoal Duo 1 will be presented at a future medical congress, the company said.

Sanofi Press Release, Dec. 2011

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This article originally posted 15 December, 2011 and appeared in  MedicationType 2 DiabetesGLP-1 AgonistIssue 604

Past five issues: Issue 626 | Special Edition - Getting Patients on Track | Diabetes Clinical Mastery Series Issue 84 | Issue 625 | Diabetes Clinical Mastery Series Issue 83 |

 
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