LivingGLP1
Study S001587

A Randomised, Double-blind, Placebo-controlled Trial to Assess Safety, Tolerability and Pharmacokinetics of Liraglutide in Obese Adolescent Subjects Aged 12 to 17 Years

Registration

Registration
NCT01789086
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
21
Start
2013-02
Primary completion
2014-05
Lead sponsor
Novo Nordisk A/S
Conditions
Metabolism and Nutrition Disorder; Obesity
Interventions
DRUG:liraglutide; DRUG:placebo
Results posted
FALSE
Secondary identifiers
EUDRACT_NUMBER:2012-000038-20; OTHER:U1111-1126-8119

Registered primary outcomes

  • Number of treatment emergent adverse events (TEAEs) [From the time of first dosing (Day 0) and until completion of follow-up visit (up to 6 weeks' treatment and 5-14 days subsequent follow-up period)]

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
R0025826Liraglutide in an Adolescent Population with Obesity: A Randomized, Double-Blind, Placebo-Controlled 5-Week Trial to Assess Safety, Tolerability, and Pharmacokinetics of Liraglutide in Adolescents Aged 12-17 Years.
Danne T, The Journal of pediatrics
2017Randomized trialPMID 27979579DOIcites ClinicalTrials.gov:NCT01789086; registry reference RESULT:27979579