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The bigger question is not how soon theyll be prescribed, but how responsibly, Ms

In a once-daily multiple ascending dose phase Ib clinical trial and a 41-day phase IIa trial in overweight and type 2 diabetic patients, general safety and tolerability of MEDI0382 were established, as well as placebo-corrected efficacy in reducing fasting blood glucose (1.7 mmol/L), post-prandial glucose excursions following a mixed meal test (22.6% AUC 04 h ), body weight (2.1 kg), and liver fat (19.6%) [7]

Owens DR, Monnier L, Hanefeld M

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Finally, in the ELIXA trial, the GLP-1 receptor agonist lixisenatide was shown to reduce UACR by 39% in people with macroalbuminuria at baseline, despite very modest effects on hemoglobin A 1c (0.3%) and body weight (0.7 kg) (13)

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