LivingGLP1
Study S000117

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

Registration

Registration
NCT01272973
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
96
Start
2011-01
Primary completion
2011-07
Lead sponsor
Novo Nordisk A/S
Conditions
Diabetes; Diabetes Mellitus, Type 2; Healthy
Interventions
DRUG:semaglutide; DRUG:placebo
Results posted
FALSE
Secondary identifiers
OTHER:U1111-1118-0257; EUDRACT_NUMBER:2010-019951-23

Registered primary outcomes

  • Frequency of adverse events (AEs) [from the first trial related activity (screening visit) and until completion of the post treatment follow-up visit 91-105 days after first dose]

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