Study S001657
Investigation of Pharmacokinetics of Two Different Presentations of Cagrilintide in Participants With Overweight and Obesity
Registration
Registered primary outcomes
- AUCss: area under the total cagrilintide concentration-time curve at steady state after 5th dosing of cagrilintide [From Pre-dose at Day 29 to Day 36]
- Cmax,ss: maximum observed concentration of total cagrilintide at steady state after 5th dosing of cagrilintide [From Pre-dose at Day 29 to Day 36]
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