LivingGLP1
Study S003207

Investigation of Pharmacokinetics, Safety and Tolerability of a Single Subcutaneous Dose of NNC0487-0111 in Participants With Various Degrees of Renal Impairment and Normal Renal Function

Registration

Registration
NCT06559527
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
42
Start
2024-08-20
Primary completion
2025-02-24
Lead sponsor
Novo Nordisk A/S
Conditions
Diabetes Mellitus, Type 2; Obesity; Overweight
Interventions
DRUG:NNC0487-0111
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1298-6886; OTHER:2023-509961-19; NIH:2023

Registered primary outcomes

  • AUC0111,0-∞,SD: Area under the NNC0487-0111 plasma concentration-time curve from time 0 to infinity after a single dose [From baseline (Visit 2, Day 1, pre-dose) until completion of the end of study visit (Visit 9, Day 28)]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0029656Renal Impairment Does Not Affect Pharmacokinetics, Safety or Tolerability of Zenagamtide.
Oldenburg LIK, Diabetes, obesity & metabolism
2026Other trialPMID 42443140DOIcites ClinicalTrials.gov:NCT06559527; registry reference DERIVED:42443140