LivingGLP1
Study S001888

A Single-centre, Parallel-group, Randomised, Double-blind, Placebocontrolled, Multiple-dose Trial to Assess the Pharmacokinetics, Pharmacodynamics, and the Safety and Tolerability of Semaglutide in Healthy Male Japanese and Caucasian Subjects

Registration

Registration
NCT02146079
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
44
Start
2014-05-21
Primary completion
2014-10-20
Lead sponsor
Novo Nordisk A/S
Conditions
Diabetes; Diabetes Mellitus, Type 2; Healthy
Interventions
DRUG:semaglutide; DRUG:placebo
Results posted
FALSE
Secondary identifiers
OTHER:U1111-1147-6660; REGISTRY:JapicCTI-142550

Registered primary outcomes

  • Area under the plasma semaglutide concentration-time curve [During a dosing interval (0-168 hours) at steady state]

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
R0020993A Randomized Trial Investigating the Pharmacokinetics, Pharmacodynamics, and Safety of Subcutaneous Semaglutide Once-Weekly in Healthy Male Japanese and Caucasian Subjects.
Ikushima I, Advances in therapy
2018Randomized trialPMID 29536338DOIcites ClinicalTrials.gov:NCT02146079; cites JapicCTI:JAPICCTI-142550; registry reference RESULT:29536338