LivingGLP1
Study S002544

Evaluation of Optimal Dosing Conditions for GLP-1 Analogue NNC0113-0987 When Administered Orally in Healthy Male Subjects

Registration

Registration
NCT02094521
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
122
Start
2014-03
Primary completion
2014-07
Lead sponsor
Novo Nordisk A/S
Conditions
Diabetes; Healthy
Interventions
DRUG:NNC0113-0987
Results posted
FALSE
Secondary identifiers
EUDRACT_NUMBER:2012-003855-13; OTHER:U1111-1133-7097

Registered primary outcomes

  • Area under the NNC0113-0987 plasma concentration time curve [From time 0 to 24 hours after the 10th dosing]

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