LivingGLP1
Study S002770

An Open-label Trial Investigating the Pharmacokinetics and the Tolerability of NNC0174-0833 in Subjects With Normal Renal Function and Impaired Renal Function

Registration

Registration
NCT04209049
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
33
Start
2020-01-15
Primary completion
2021-01-05
Lead sponsor
Novo Nordisk A/S
Conditions
Overweight; Obesity
Interventions
DRUG:NNC0174-0833
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1228-9001

Registered primary outcomes

  • Area under the plasma NNC0174-0833 concentration-time curve after a single dose [From baseline (Visit 2, Day 1, pre-dose) until completion of the end of trial visit (Visit 7, Day 36)]

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
R0003002Renal or Hepatic Impairment Does Not Affect Pharmacokinetics, Safety, or Tolerability of Subcutaneous Cagrilintide.
Nielsen MJF, Clinical pharmacokinetics
2026Other trialPMID 42228334DOIcites ClinicalTrials.gov:NCT04209049; registry reference DERIVED:42228334