Study S000890
Bioequivalence Study of Cagrilintide B + Placebo Semaglutide I and Cagrilintide D Once Weekly in Participants With Overweight or Obesity
Registration
Registered primary outcomes
- AUC,ss: area under the total cagrilintide concentration-time curve at steady state after 5th dosing of cagrilintide s.c. [Day 113 (pre-dose) to Day 120 (post-dose)]
- Cmax,ss: maximum concentration of total cagrilintide at steady state after 5th dosing of cagrilintide s.c. [Day 113 (pre-dose) to Day 120 (post-dose)]
Linked records (0)
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