LivingGLP1
Study S003212

Investigation of Safety, Tolerability and Pharmacokinetic Properties of Single Doses of Subcutaneous NNC0487-0111 in Chinese Participants With Overweight or Obesity.

Registration

Registration
NCT07121153
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
36
Start
2025-08-11
Primary completion
2025-12-20
Lead sponsor
Novo Nordisk A/S
Conditions
Overweight; Obesity
Interventions
DRUG:NNC0487-0111 A; DRUG:Placebo A
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1311-5582

Registered primary outcomes

  • Number of treatment emergent adverse events (TEAEs) [From NNC0487-0111 administration (Day 1) to completion of the end of study visit (Day 23)]

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