LivingGLP1
Study S001657

Investigation of Pharmacokinetics of Two Different Presentations of Cagrilintide in Participants With Overweight and Obesity

Registration

Registration
NCT07605052
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
50
Start
2026-05-20
Primary completion
2026-08-19
Lead sponsor
Novo Nordisk A/S
Conditions
Overweight; Obesity
Interventions
DRUG:Cagrilintide B; DRUG:Cagrilintide D
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1336-5994

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]

Linked records (0)

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