LivingGLP1
Study S001655

Investigation of Safety, Tolerability and Pharmacokinetics of Subcutaneously Co-administered Single Doses of NNC0480-0389 and Semaglutide in Healthy Japanese Male Subjects

Registration

Registration
NCT04878406
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
24
Start
2021-05-18
Primary completion
2021-07-20
Lead sponsor
Novo Nordisk A/S
Conditions
Healthy Volunteers Type 2 Diabetes
Interventions
DRUG:NNC0480-0389; DRUG:Placebo (NNC0480-0389); DRUG:Semaglutide; DRUG:Placebo (Semaglutide)
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1263-7182

Registered primary outcomes

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

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