LivingGLP1
Study S000831

A Study Comparing Exposure of Semaglutide and Dapagliflozin Dosed Orally as Mono-components Versus in a Fixed-dose Combination

Registration

Registration
NCT05429593
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
152
Start
2022-06-22
Primary completion
2023-03-10
Lead sponsor
Novo Nordisk A/S
Conditions
Healthy Volunteers
Interventions
DRUG:Semaglutide; DRUG:Dapagliflozin; DRUG:Semaglutide/dapagliflozin
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1266-4254; OTHER:2022-500007-52-00

Registered primary outcomes

  • AUC0-24h,sema,ss: area under the semaglutide plasma concentration-time curve during a dosing interval (0 to 24 hours) at steady state [From 0 to 24 hours on day 49 and 84 in Part 1]
  • AUC0-24h,dapa,ss: area under the dapagliflozin plasma concentration-time curve during a dosing interval (0 to 24 hours) at steady state [From 0 to 24 hours on day 49 and 98 in Part 2]

Linked records (0)

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