LivingGLP1
Study S000848

A Single Centre, Multiple Dose, Open Label Randomised Trial to Evaluate the Effect of Post Dose Meal Timings and the Effect of Volume of Water With Dosing on the Pharmacokinetic Properties of Oral Semaglutide in Healthy Male Subjects

Registration

Registration
NCT01572753
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
161
Start
2012-04-12
Primary completion
2012-09-08
Lead sponsor
Novo Nordisk A/S
Conditions
Diabetes; Diabetes Mellitus, Type 2; Healthy
Interventions
DRUG:semaglutide
Results posted
FALSE
Secondary identifiers
EUDRACT_NUMBER:2010-019653-17; OTHER:U1111-1120-6776

Registered primary outcomes

  • AUC 0-24h; Area under the semaglutide concentration curve from time 0-24 hours after the 10th dosing [0-24hrs after the 10th dosing]

Linked records (2)

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
R0011209Clinical Pharmacokinetics of Oral Semaglutide: Analyses of Data from Clinical Pharmacology Trials.
Overgaard RV, Clinical pharmacokinetics
2021Other trialPMID 33969456DOIcites ClinicalTrials.gov:NCT01572753; registry reference DERIVED:33969456
R0015802Effect of Various Dosing Conditions on the Pharmacokinetics of Oral Semaglutide, a Human Glucagon-Like Peptide-1 Analogue in a Tablet Formulation.
Bækdal TA, Diabetes therapy : research, treatment and education of diabetes and related disorders
2021Randomized trialPMID 34080123DOIcites ClinicalTrials.gov:NCT01572753; registry reference DERIVED:34080123