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Description

doi:10.1172/JCI112855

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European Medicines Agency (EMA) Eli Lilly typically files for European approval (through the EMA's centralized procedure) around the same time as the FDA submission, sometimes within a few months

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In the same line, Fujita et al described a patient on chronic hydrocortisone who manifested symptoms of hypocortisolism after the start of exenatide therapy [33]

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References: Wilding, J

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In conclusion, we have identified molecular and cellular targets for GLP-1(2836) in the cardiovascular system

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