A Research Study Comparing How Well Different Doses of the Medicine NNC0487-0111 Lower Blood Sugar in People With Type 2 Diabetes

Part of paid clinical trials in Santa Ana, California.

Sponsor
Novo Nordisk A/S
Study ID
NCT06542874
Phase
PHASE2
Status
Completed

Conditions

  • Type 2 Diabetes (T2D)

Eligibility Criteria

Sex
ALL
Age
18 Years - 75 Years
Healthy Volunteers
Not accepted

Interventions

Study Details

The study will look at how well different doses of a new medicine called NNC0487-0111 help lower the blood sugar and body weight in people with type 2 diabetes. NNC0487-0111 is a new medicine which cannot be prescribed by doctors but has previously been tested in humans. Participants will either get NNC0487-0111, which is given as tablets or as injections, or placebo. Which treatment the participant get is decided by chance.The study will last for about 43 weeks.

Key Dates

Start date
Aug 7, 2024
Status verified
Dec 2025
Primary completion
Oct 1, 2025
Completion
Oct 24, 2025

Study Design

Enrollment
448 participants (actual)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Placebo Comparator: Placebo subcutaneous
    Placebo for subcutaneous treatment
  • Experimental: NNC0487-0111 subcutaneous dose 1
    NNC0487-0111 subcutaneous dose 1 treatment
  • Experimental: NNC0487-0111 subcutaneous dose 2
    NNC0487-0111 subcutaneous dose 2 treatment
  • Experimental: NNC0487-0111 subcutaneous dose 3
    NNC0487-0111 subcutaneous dose 3 treatment
  • Experimental: NNC0487-0111 subcutaneous dose 4
    NNC0487-0111 subcutaneous dose 4 treatment
  • Experimental: NNC0487-0111 subcutaneous dose 5
    NNC0487-0111 subcutaneous dose 5 treatment
  • Experimental: NNC0487-0111 subcutaneous dose 6
    NNC0487-0111 subcutaneous dose 6 treatment
  • Placebo Comparator: Placebo oral
    Placebo for oral treatment
  • Experimental: NNC0487-0111 oral dose 1
    NNC0487-0111 oral dose 1 treatment
  • Experimental: NNC0487-0111 oral dose 2
    NNC0487-0111 oral dose 2 treatment
  • Experimental: NNC0487-0111 oral dose 3
    NNC0487-0111 oral dose 3 treatment

Primary Outcome Measure

Change in HbA1c [ Time Frame: From baseline (week 0) to end of treatment (week 36) ]

Locations (28)

FacilityCityStateZIP
Southern Cal Clinical ResearchSanta AnaCalifornia92701
Chase Medical Research LLCWaterburyConnecticut06708
Fleming Island Ctr for Clin ResFleming IslandFlorida32003
Encore Medical Research LLCHollywoodFlorida33024
South Broward Research LLCMiramarFlorida33027
Florida Inst For Clin ResOrlandoFlorida32825
Cedar-Crosse Research CenterChicagoIllinois60607
Advanced Internal Medicine, PLLCPaducahKentucky42001
Medstar Research Institute_HyattsvilleHyattsvilleMaryland20782
MD Medical ResearchOxon HillMaryland20745
Arcturus HC PLC Troy Med ResTroyMichigan48098
Arcturus Healthcare, PLCTroyMichigan48098
Clinical Research ProfessionalsChesterfieldMissouri63005
AMC Community EndocrinologyAlbanyNew York12203
Lucas Research Inc.Morehead CityNorth Carolina28557
Piedmont Healthcare/ResearchStatesvilleNorth Carolina28625
Plains Clinical Research Center, LLC_FargoFargoNorth Dakota58104
Preferred Primary Care Physicians_PittsburghPittsburghPennsylvania15236
Health ConceptsRapid CitySouth Dakota57702
Clinical Research AssociatesNashvilleTennessee37203
MidState Endocrine AssociatesNashvilleTennessee37203
Velocity Clinical Res-DallasDallasTexas75230
PlanIt Research, PLLCHoustonTexas77079
Synergy Groups MedicalHoustonTexas77061
Victorium Clinical ResearchHoustonTexas77024
Radiance Clinical ResearchLampasasTexas76550
Tekton ResearchMcKinneyTexas75069
Hillcrest Family Health CenterWacoTexas76708

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