LivingGLP1
Study S001070

Oral Semaglutide Pharmacokinetics in Healthy Subjects, Effect of Dosing Schedules

Registration

Registration
NCT04513704
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
156
Start
2020-08-28
Primary completion
2021-04-20
Lead sponsor
Novo Nordisk A/S
Conditions
Healthy Volunteers Type 2 Diabetes
Interventions
DRUG:Oral Semaglutide
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1243-9641; REGISTRY:2019-004569-42; NIH:2019

Registered primary outcomes

  • Area under the semaglutide plasma concentration - time curve during a dosing interval after the 10th dosing (AUC0-24h,sema,day10) [From 0 to 24 hours after the 10th dosing (day 10)]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0015924Effect of Various Dosing Schedules on the Pharmacokinetics of Oral Semaglutide: A Randomised Trial in Healthy Subjects.
van Hout M, Clinical pharmacokinetics
2023Randomized trialPMID 36932262DOIcites ClinicalTrials.gov:NCT04513704; registry reference DERIVED:36932262