Overview

A Research Study of a New Medicine NNC0519-0130 in Japanese and Non-Japanese Men

Status:
Not yet recruiting
Trial end date:
2023-11-14
Target enrollment:
0
Participant gender:
Male
Summary
NNC0519-0130 is a new medicine which may possibly help participants with type 2 diabetes. This study, will look into how safe the new medicine NNC0519-0130 is, and we will measure its concentrations in the blood and look at its effects. This study will last for a maximum of 19 weeks and Japanese and Non-Japanese male participants will be included.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Novo Nordisk A/S
Criteria
Inclusion Criteria:

- Body mass index (BMI) between 23.0 kilogram per meter square (kg/m^2) and 39.9 kg/m^2
(both inclusive) at screening with a minimum weight of 50 kilogram (kg). 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 (ECG) and clinical laboratory tests
performed during the screening visit, as judged by the investigator.

- For Japanese participants: Both parents of Japanese descent.

- For non-Japanese participants in the oral study part: Both parents of non-Japanese
descent. Minimum 60% of participants should have parents of Caucasian descent while a
maximum of 40% can have parents of Hispanic or African descent.

- For non-Japanese participants in the s.c. study part: Both parents of Caucasian
descent.

Exclusion Criteria:

- 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.

- Glycosylated haemglobin (HbA1c) greater than or equal to 6.5 percent (48 millimoles
per mole [mmol/mol]) at screening.

- Use of prescription medicinal products or non-prescription drugs, except routine
vitamins, occasional use of paracetamol, ibuprofen, acetylsalicylic acid (ASA), and
domperidon, or topical medication not reaching systemic circulation, within 14 days
before screening.