First Research Study of the Possible New Medicine NNC0113-2023 in Healthy Men.

Phase 1

Completed

Brief Summary: The aim of this study is to assess how safe the study drug is and how well a participant tolerates it after a single oral (taken by mouth) dose. The study also aims to measure the concentration of the study drug and its breakdown products after a single dose. Participants will either get NNC0113-2023 (a new medicine) or placebo (a "dummy medicine similar to the study medicine but without active ingredients) - which treatment any participant gets is decided by chance. Participants will get one dose (can be one or two tablets) of study medicine. The study will last for about 65 days. Participants will have 10 scheduled site visits with the study physician or study staff at the study centre. For one of the visits, participants will stay at the research unit for 5 days. At all visits, except the first information visit, participants will have blood drawn along with other clinical assessments. Participants cannot take part in this study if participants have any disorder that the doctor thinks is a health problem. Only healthy men are allowed to take part.

Recruitment & Eligibility

Inclusion Criteria

Male aged 18 - 45 years (both inclusive) at the time of signing informed consent.
Body mass index between 20.0 kg/m^2 and 29.9 kg/m^2 (both inclusive).
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.

Exclusion Criteria

HbA1c greater than or equal to 6.5 % (48 mmol/mol) at screening.
Use of tobacco and nicotine products, defined as any of the below: 1) Smoking more than 1 cigarettes or the equivalent per day or 2) Not willing to refrain from smoking and use of nicotine substitute products during the in-house period.
History of major surgical procedures involving the stomach potentially affecting absorption of trial products (e.g. subtotal and total gastrectomy, sleeve gastrectomy, gastric bypass surgery).
Presence of clinically significant gastrointestinal disorders or symptoms of gastrointestinal disorders potentially affecting absorption of drugs or nutrients, as judged by the investigator.
Personal or first degree relative(s) history of multiple endocrine neoplasia type 2 or medullary thyroid carcinoma.
Presence or history of pancreatitis (acute or chronic).

Arm && Interventions

Group	Intervention	Description
Placebo	Placebo (NNC0113-2023)	Participants will receive placebo (NNC0113-2023)
NNC0113-2023	NNC0113-2023	Participants will receive increasing doses of NNC0113-2023 on day 1. Each participant will receive only a single dose.

Primary Outcome Measures

Name	Time	Method
Number of treatment emergent adverse events (TEAEs)	From time of dosing (day 1) until completion of the follow-up visit (day 43)	Count of events

Secondary Outcome Measures

Name	Time	Method
AUC0-24h,SNAC,SD; the area under the SNAC plasma concentration-time curve from time 0 to 24 hours after a single dose of oral NNC0113-2023	From baseline (day 1) to 24 hours after dosing	Measured in ng/mL\*h
Cmax,SNAC,SD; the maximum plasma concentration of SNAC in plasma after a single dose of oral NNC0113-2023	From baseline (day 1) to 24 hours after dosing	Measured in ng/mL
AUC0-∞,2023,SD; the area under the NNC0113-2023 plasma concentration-time curve from time 0 to infinity after a single dose of oral NNC0113-2023	From baseline (day 1) to post treatment follow-up (day 43)	Measured in nmol/L\*h
Cmax,2023,SD; the maximum plasma concentration of NNC0113-2023 after a single dose of oral NNC0113-2023	From baseline (day 1) to post treatment follow-up (day 43)	Measured in nmol/L

Locations (1): Novo Nordisk Investigational Site
🇺🇸
San Antonio, Texas, United States

Receive instant email notifications about changes in this clinical trial

Receive instant email notifications about changes in this clinical trial