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Potential limitations of both studies include the use of a single dose rather than multiple doses of cagrilintide and the use of doses (0.6 mg in the renal impairment study and 0.9 mg in the hepatic impairment study) lower than the 2.4 mg dose being evaluated in clinical development

Studies use it to examine the lipolytic activity localized to the C-terminal domain of growth hormone, independent of the growth-promoting and glucose-related actions of the full-length hormone

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