LivingGLP1
Study S000012

Investigation of the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single and Multiple Doses of NNC0480-0389 in Combination With Semaglutide s.c.

Registration

Registration
NCT04259801
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
152
Start
2020-02-17
Primary completion
2022-03-16
Lead sponsor
Novo Nordisk A/S
Conditions
Healthy Volunteers; Overweight; Obesity; Diabetes Mellitus, Type 2
Interventions
DRUG:NNC0480-0389; DRUG:Semaglutide; DRUG:Placebo (NNC0480-0389); DRUG:Placebo (semaglutide)
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
REGISTRY:2019-002857-44; OTHER:U1111-1236-4114; NIH:2019

Registered primary outcomes

  • Number of treatment emergent adverse events (TEAE) in Part 1 [From time of dosing (day 1) until completion of follow-up visit (day 71)]
  • Number of treatment emergent adverse events (TEAE) in Part 2 [From first combination dosing (day 57) until completion of follow-up visit (day 148)]

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