LivingGLP1
Study S001254

Investigation of the Effect of Dosing Conditions on the Pharmacokinetics of New Oral Semaglutide Formulation in Healthy Participants

Registration

Registration
NCT05996874
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
121
Start
2023-08-12
Primary completion
2024-04-18
Lead sponsor
Novo Nordisk A/S
Conditions
Healthy Participants
Interventions
DRUG:Semaglutide
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1281-4819; EUDRACT_NUMBER:2022-002848-52

Registered primary outcomes

  • AUC0-24h,sema,Day10: Area under the semaglutide plasma concentration-time curve during a dosing interval after the 10th dosing [From 0 to 24 hours after dosing on day 10]

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