LivingGLP1
Study S000870

Investigation of Pharmacokinetics, Safety and Tolerability of Oral Semaglutide in Subjects With Various Degrees of Impaired Renal Function Compared to Subjects With Normal Renal Function

Registration

Registration
NCT02014259
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
71
Start
2013-12-11
Primary completion
2014-10-24
Lead sponsor
Novo Nordisk A/S
Conditions
Diabetes; Diabetes Mellitus, Type 2; Healthy
Interventions
DRUG:semaglutide
Results posted
FALSE
Secondary identifiers
EUDRACT_NUMBER:2013-000682-36; OTHER:U1111-1139-4281

Registered primary outcomes

  • Area under the semaglutide plasma concentration time curve [From time 0 to 24 hours 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:NCT02014259
R0017720Pharmacokinetics, Safety and Tolerability of Oral Semaglutide in Subjects with Renal Impairment.
Granhall C, Clinical pharmacokinetics
2018Other trialPMID 29623579DOIcites ClinicalTrials.gov:NCT02014259; registry reference RESULT:29623579