LivingGLP1
Study S000890

Bioequivalence Study of Cagrilintide B + Placebo Semaglutide I and Cagrilintide D Once Weekly in Participants With Overweight or Obesity

Registration

Registration
NCT07597018
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
RECRUITING
Enrollment
234
Start
2026-05-18
Primary completion
2027-05-28
Lead sponsor
Novo Nordisk A/S
Conditions
Obesity; Overweight
Interventions
DRUG:Cagrilintide D; DRUG:Cagrilintide B and placebo semaglutide I
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1314-9337; OTHER:2025-521384-12; NIH:2025

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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