LivingGLP1
Study S000720

A Study Investigating the Pharmacokinetic Properties When Dosing Different Formulations of Semaglutide to Healthy Male Participants - Oral Formulation III

Registration

Registration
NCT06097390
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
121
Start
2023-09-28
Primary completion
2024-02-22
Lead sponsor
Novo Nordisk A/S
Conditions
Healthy Participants
Interventions
DRUG:Semaglutide
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1289-1040

Registered primary outcomes

  • Adjusted AUC0-24h,sema; adjusted area under the semaglutide plasma concentration-time curve [From 0 to 24 hours after dosing on day 80 and 90]

Linked records (0)

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