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Accordingly, it is preferred that the solid oral pharmaceutical composition has a dissolution profile, as determined by the dissolution method according to USP, with less than 5% of the GLP-1 receptor agonist released within 1 hour in simulated gastric fluid, followed by dissolution in simulated intestinal fluid at pH between 6 and 6.5 with a lag time of at least 1 hour, whereby not more than 10% of the GLP-1 receptor agonist is released within the lag time, and whereby after the lag time more than 75% of the GLP-1 receptor agonist is released in simulated intestinal fluid at pH between 6 and 6.5 within 1 hour

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She also pushed back on the argument that patients are getting these anyway