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)

FacilityCityStateZIPSite coordinators
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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