LivingGLP1
Study S000224

Investigation on Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Doses of a Long-acting GLP-1 Analogue in Healthy Male Subjects and Male Subjects With Type 2 Diabetes

Registration

Registration
NCT01686945
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
107
Start
2012-09-19
Primary completion
2013-04-08
Lead sponsor
Novo Nordisk A/S
Conditions
Diabetes; Diabetes Mellitus, Type 2; Healthy
Interventions
DRUG:semaglutide; DRUG:placebo
Results posted
FALSE
Secondary identifiers
EUDRACT_NUMBER:2012-000361-20; OTHER:U1111-1127-4408

Registered primary outcomes

  • Number of treatment emergent adverse events (TEAEs) recorded [From the time of first dosing and until completion of the post treatment follow-up visits (Day 90 to 104)]

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
R0016569Safety and Pharmacokinetics of Single and Multiple Ascending Doses of the Novel Oral Human GLP-1 Analogue, Oral Semaglutide, in Healthy Subjects and Subjects with Type 2 Diabetes.
Granhall C, Clinical pharmacokinetics
2019Randomized trialPMID 30565096DOIcites ClinicalTrials.gov:NCT01686945; registry reference DERIVED:30565096