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10.3390/antiox12081553 19 ChintaS
The results were negative or ambiguous
These symptoms reflect adrenergic hypersensitivity and calcium dysregulation (88, 89)
Figure 1: Changes in body weight from baseline to the end of treatment at week 26 associated with the trial product estimand, in the randomly assigned treatment groups administered either 0.3 mg of cagrilintide, 0.6 mg of cagrilintide, 1.2 mg of cagrilintide, 2.5 mg of cagrilintide, 4.5 mg of cagrilintide, 3.0 mg of liraglutide, or a placebo
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