LivingGLP1
Study S001558

Investigation of Safety, Tolerability and Pharmacokinetic Properties of Multiple Doses of Oral NNC0487-0111 in Japanese Participants With Obesity

Registration

Registration
NCT06049329
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
36
Start
2023-09-14
Primary completion
2023-12-15
Lead sponsor
Novo Nordisk A/S
Conditions
Obesity
Interventions
DRUG:NNC0487-0111; DRUG:Placebo (NNC0487-0111)
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1284-5901

Registered primary outcomes

  • Number of treatment emergent adverse events (TEAE) [From pre-dose on Day 1 until completion of the end of study visit Day 31]

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