| Trial ID: | L4239 |
| Source ID: | NCT06567041
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| Associated Drug: |
Nnc0519-0130
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| Title: |
A Research Study of How Safe a New Medicine Called NNC0519 0130 is and to Test Its Effect in People Living With Excess Body Weight With or Without Type 2 Diabetes
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| Acronym: |
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| Status: |
ACTIVE_NOT_RECRUITING
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| Study Results: |
NO
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| Results: |
|
| Conditions: |
Diabetes Mellitus, Type 2|Obesity
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| Interventions: |
DRUG: NNC0519-0130|DRUG: Placebo
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| Outcome Measures: |
Primary: Number of adverse events, Measured in number of events., From time of first dosing (day 1) until completion of the end of study visit (day 274/253) | Secondary: Change in 12-lead electrocardiogram, Individual-specific heart rate corrected QT interval (QTcI), Measured in milliseconds (ms)., From baseline (day - 1) until completion of the end of study visit (day 274/253)|Change in 12-lead electrocardiogram, Fridericia heart rate corrected QT interval (QTcF), Measured in ms., From baseline (day - 1) until completion of the end of study visit (day 274/253)|Area under the NNC0519-0130 plasma concentration-time curve in steady state, Measured in hours\*nanomoles per liter (h\*nmol/L)., From pre-dose until 7 days post-dose, for third and last doses in the maintenance period|Maximum plasma concentration of NNC0519-0130 in steady state, Measured in nanomoles per liter (nmol/L)., From pre-dose until 7 days post-dose, for third and last doses in the maintenance period
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| Sponsor/Collaborators: |
Sponsor: Novo Nordisk A/S
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| Gender: |
ALL
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| Age: |
ADULT
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| Phases: |
PHASE1
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| Enrollment: |
64
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| Study Type: |
INTERVENTIONAL
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| Study Designs: |
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
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| Start Date: |
2024-08-07
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| Completion Date: |
2025-12-03
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| Results First Posted: |
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| Last Update Posted: |
2025-04-10
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| Locations: |
Parexel International GmbH, Berlin, 14050, Germany
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| URL: |
https://clinicaltrials.gov/show/NCT06567041
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