Study S003212
Investigation of Safety, Tolerability and Pharmacokinetic Properties of Single Doses of Subcutaneous NNC0487-0111 in Chinese Participants With Overweight or Obesity.
Registration
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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