This study is testing a new medicine, NNC6989-0001, to test it is safe and tolerable for healthy people living with overweight or obesity. NNC6989-0001 is still being tested in studies and is not yet available for prescription by doctors. In this study, participants will receive either NNC6989-0001 or a placebo; which treatment each participant receives will be decided by chance.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
96
Participants assigned to the active intervention receive NNC6989-0001 A
Participants assigned to the placebo, receive placebo matched in appearance to the active drug.
ICON Early Phase Services, LLC
Lenexa, Kansas, United States
RECRUITINGNumber of treatment emergent adverse events (TEAE) - Part A
Measure in number of events.
Time frame: From time of dosing on Day1 until completion of the end of study visit (Day 7)
Number of treatment emergent adverse events (TEAE) - Part B
Measured in number of events
Time frame: From time of dosing on Day 1 until completion of the end of study visit (Day 14)
AUC; the area under the NNC6989-0001 plasma concentration-time curve - Part A
Measured in hours times nanograms per millilitre(h\*ng/ml).
Time frame: From pre-dose on Day 1 until completion of the end of study visit (Day 7)
Cmax; the maximum plasma concentration of NNC6989-0001 - Part A
Measured in nanograms per millilitre(ng/ml).
Time frame: From pre-dose on Day 1 until completion of the end of study visit (Day 7)
AUC; the area under the NNC6989-0001 plasma concentration-time curve - Part B
Measured in h\*ng/ml.
Time frame: From pre-dose on Day 1 until completion of the end of study visit (Day 14)
Cmax; the maximum plasma concentration of NNC6989-0001 - Part B
Measured in ng/ml.
Time frame: From pre-dose on Day 1 until completion of the end of study visit (Day 14)
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