Study S003388
Investigation of the Pharmacokinetics of Subcutaneously Administered NNC0480-0389 in Participants With Various Degrees of Impaired Renal Function Compared to Participants With Normal Renal Function
Registration
Registered primary outcomes
- AUC0-∞,NNC0480-0389,SD, area under the NNC0480-0389 plasma concentration time curve after a single dose [From baseline (visit 2, day 1, pre-dose) until completion of the end-of-study visit (visit 11, day 36)]
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