LivingGLP1
Study S000858

A Randomised, Double-blind, Placebo-controlled Trial to Assess Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Liraglutide in Obese Children Aged 7 to 11 Years

Registration

Registration
NCT02696148
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
24
Start
2016-03-14
Primary completion
2017-04-13
Lead sponsor
Novo Nordisk A/S
Conditions
Metabolism and Nutrition Disorder; Obesity
Interventions
DRUG:liraglutide; DRUG:placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1162-9171; EUDRACT_NUMBER:2014-004454-34; NIH:2014

Registered primary outcomes

  • Number of treatment emergent adverse events [From the time of first dosing and until completion of follow-up visit (59-108 days after first dosing)]

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
R0024666Liraglutide effects in a paediatric (7-11 y) population with obesity: A randomized, double-blind, placebo-controlled, short-term trial to assess safety, tolerability, pharmacokinetics, and pharmacodynamics.
Mastrandrea LD, Pediatric obesity
2019Randomized trialPMID 30653847DOIregistry reference RESULT:30653847