LivingGLP1
Study S000626

A Trial Comparing Exposure of Semaglutide When Dosing New Formulations of Oral Semaglutide to Healthy Male Subjects

Registration

Registration
NCT03638778
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
105
Start
2018-08-17
Primary completion
2018-12-05
Lead sponsor
Novo Nordisk A/S
Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG:Semaglutide 3 mg; DRUG:Semaglutide 7 mg; DRUG:Semaglutide B 3 mg; DRUG:Semaglutide B 7 mg; DRUG:Semaglutide C 3 mg; DRUG:Semaglutide C 7 mg; DRUG:Semaglutide D 3 mg; DRUG:Semaglutide D 7 mg
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1206-6210; REGISTRY:2017-005023-24; NIH:2017

Registered primary outcomes

  • AUC0-24h,sema,day10, area under the semaglutide plasma concentration time curve from 0 to 24 hours after the 10th dosing [0 to 24 hours on day 10]

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