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Compliance of 130% was considered as non-compliant and any subject demonstrating non-compliance for two consecutive visits was withdrawn from the study

Once a manufacturer submits an EUA request for a COVID-19 vaccine to the FDA, the agency then evaluates the request and determines whether the relevant statutory criteria are met, taking into account the totality of the scientific evidence about the vaccine that is available to the FDA

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Evaluating the effects of the novel GLP-1 analogue liraglutide in Alzheimers disease: Study protocol for a randomised controlled trial (ELAD study)