LivingGLP1
Study S003214

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

Registration

Registration
NCT06820476
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
29
Start
2025-02-09
Primary completion
2025-05-14
Lead sponsor
Novo Nordisk A/S
Conditions
Overweight; Obesity
Interventions
DRUG:NNC0487-0111; DRUG:Placebo (NNC0487-0111)
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1289-3164

Registered primary outcomes

  • Number of treatment emergent adverse events (TEAEs) [From first NNC0487-0111 administration (Day 1) to completion of the end-of-study visit (Day 31)]

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