LivingGLP1
Study S002769

Investigation on Safety, Tolerability and Pharmacokinetics of Single Doses of NNC0174-0833 in Normal Weight, Overweight to Obese But Otherwise Healthy Male Subjects

Registration

Registration
NCT02300844
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
54
Start
2014-12-01
Primary completion
2016-03-21
Lead sponsor
Novo Nordisk A/S
Conditions
Metabolism and Nutrition Disorder; Obesity
Interventions
DRUG:NNC0174-0833; DRUG:placebo
Results posted
FALSE
Secondary identifiers
OTHER:U1111-1131-7160

Registered primary outcomes

  • Number of treatment emergent adverse events (TEAEs) [From the time of dosing (Day 1) until completion of the post treatment follow-up visit (Day 43-50)]

Linked records (0)

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