A Research Study of a New Medicine NNC0519-0130 in Healthy People, People With High Body Weight and People With Type 2 Diabetes.

Korábbi kezelés

• Use of prescription medicinal products or non-prescription drugs, except routine vitamins, occasional use of paracetamol, ibuprofen, acetylsalicylic acid, and domperidon, or topical medication not reaching systemic circulation, within 14 days before screening
• Use of prescription medicinal products or non-prescription drugs, except routine vitamins, occasional use of paracetamol, ibuprofen, acetylsalicylic acid, and domperidon, or topical medication not reaching systemic circulation, within 14 days before screening
• Use of prescription medicinal products or non-prescription drugs, except routine vitamins, occasional use of paracetamol, ibuprofen, acetylsalicylic acid, and domperidon, or topical medication not reaching systemic circulation, within 14 days before screening
• Current treatment with systemically effective corticosteroids, monoamine oxidase (MAO) inhibitors, systemic non-selective beta-blockers, growth hormone, non-routine vitamins or herbal products
• Current treatment with selected oral medication with a narrow therapeutic window, such as warfarin, digoxin, tricyclic antidepressants, lithium, aminophylline, theophylline and anticonvulsants

Más betegség

• Any disorder, which in the investigator's opinion might jeopardise participant's safety or compliance with the protocol
• Any disorder, which in the investigator's opinion might jeopardise participant's safety or compliance with the protocol
• Presence or history of any clinically relevant respiratory, metabolic, renal, hepatic, cardiovascular, gastrointestinal, or endocrinological conditions
• Any disorder, which in the investigator's opinion might jeopardise participant's safety or compliance with the protocol
• Presence or history of any clinically relevant respiratory, metabolic, renal, hepatic, cardiovascular, gastrointestinal, or endocrinological conditions
• Type 2 diabetes (T2D) part:
• Any disorder, except for conditions associated with T2D, which in the investigator's opinion might jeopardise participant's safety or compliance with the protocol
• Presence or history of any clinically relevant respiratory, metabolic, renal, hepatic, gastrointestinal, endocrinological conditions (except conditions associated with diabetes mellitus)

Laborértékek

• Glycosylated haemoglobin (HbA1c) greater than or equal to (≥) 6.5 % (48 millimoles per mole (mmol/mol)) at screening
• HbA1c greater than or equal to (≥) 6.5 % (48 mmol/mol) at screening
• HbA1c greater than or equal to (≥) 6.5 % (48 mmol/mol) at screening

Egyéb

• Single ascending dose (SAD) part:
• Multiple ascending dose (MAD) part (MAD QD and MAD QW):

• Single ascending dose (SAD) part:
• Male aged 18-55 years (both inclusive) at screening
• Body mass index between 18.5 kilogram per meter square (kg/m\^2) and 27.0 kg/m\^2 (both inclusive) at screening
• Considered to be generally healthy based on the medical history, physical examination, and the results of vital signs, electrocardiogram and clinical laboratory tests performed during the screening visit, as judged by the investigator
• Multiple ascending dose (MAD) part (MAD QD and MAD QW):
• Male aged 18-55 years (both inclusive) at screening
• Body mass index between 25.0 kg/m\^2 and 39.9 kg/m\^2 (both inclusive) at screening. Overweight should be due to excess adipose tissue, as judged by the investigator
• Considered eligible based on the medical history, physical examination, and the results of vital signs, electrocardiogram and clinical laboratory tests performed during the screening visit, as judged by the investigator
• Type 2 diabetes (T2D) part:
• Female of non-childbearing potential or male aged 18-64 years (both inclusive) at screening
• Body mass index between 25.0 kg/m\^2 and 39.9 kg/m\^2 (both inclusive) at screening
• Diagnosed with type 2 diabetes mellitus greater than or equal to (≥) 180 days before screening
• Treatment naive to antidiabetic drugs or on a stable daily dose(s) of metformin therapy (any metformin formulation any dose) greater than or equal to (>=) 60 days before screening
• Insulin naive. However, short-term insulin treatment for a maximum of 14 days before screening is allowed, as is prior insulin treatment for gestational diabetes
• HbA1c in the range of 6.5% (inclusive) and 9.5% (inclusive)