LivingGLP1
Study S001082

A Randomised Trial Investigating Steady State Semaglutide Exposure of 25 and 50 mg of Oral Semaglutide in Different Formulations in Healthy Subjects

Registration

Registration
NCT04524832
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
290
Start
2020-09-29
Primary completion
2022-02-25
Lead sponsor
Novo Nordisk A/S
Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG:Oral semaglutide
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1242-2643; REGISTRY:2019-004157-80; NIH:2019

Registered primary outcomes

  • Area under the semaglutide plasma concentration - time curve during a dosing interval at steady state (AUC0-24h,sema,SS) [From 0 to 24 hours after the last dosing of oral semaglutide 25 mg on visit 8, day 84]
  • Area under the semaglutide plasma concentration-time curve during a dosing interval at steady state (AUC0-24h,sema,SS) [From 0 to 24 hours after the last dosing of oral semaglutide 50 mg on visit 10, day 112]

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