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As the discontinuation rates were also high with the twice daily danuglipron at the phase 2 obesity trial (as discussed above), twice daily danuglirpon formulation will not advance into phase 3 studies, but an improved once-daily formulation with an aim to improve tolerability profile is currently under assessment [27]
BPC-157's musculoskeletal soft-tissue work is summarized by Gwyer et al
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Inferring a specific gastric-emptying rate from a side-effect profile is a reasonable hypothesis, not a quantified result
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