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near research site (if localized SubQ modeling possible) or systemic administration for broader studies Cycle length: 46 weeks on for acute injury models (extend to 8 weeks if needed for chronic issues), followed by 24 weeks off to reset sensitivity Use strictly according to the manufacturers directions

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They did however comment in their New England Journal of Medicine article that the affinity of lixisenatide for the GLP-1 receptor was up to four times greater than that of human GLP-1and there have been neuroprotective actions shown in animal models of Alzheimers disease. Together, I suspect these were likely strong rationales driving their choice of the use of Lixisenatide