LivingGLP1
Study S001618

Investigation of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Dosing of NNC0174-0833 in Combination With Semaglutide in Subjects Being Overweight or With Obesity

Registration

Registration
NCT03600480
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
96
Start
2018-07-25
Primary completion
2020-06-12
Lead sponsor
Novo Nordisk A/S
Conditions
Obesity; Overweight
Interventions
DRUG:NNC0174-0833; DRUG:Semaglutide; DRUG:Placebo (NNC0174-0833)
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1203-6796

Registered primary outcomes

  • Number of treatment emergent adverse events (TEAEs) [From first administration of NNC0174-0833 (Day 1) to completion of the post-treatment follow-up (Day 176)]

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
R0014843Safety, tolerability, pharmacokinetics, and pharmacodynamics of concomitant administration of multiple doses of cagrilintide with semaglutide 2·4 mg for weight management: a randomised, controlled, phase 1b trial.
Enebo LB, Lancet (London, England)
2021Randomized trialPMID 33894838DOIcites ClinicalTrials.gov:NCT03600480; registry reference RESULT:33894838