A Research Study Looking at the Effect of Food Intake on How the Medicine NN0385-0434 Behaves in the Body of Healthy Participants

Phase 1

Completed

• Conditions: Healthy Volunteers; Established Atherosclerotic Cardiovascular Disease (ASCVD) or ASCVD Risk; Elevated Cholesterol
• Interventions: Drug: NNC0385-0434

• Registration Number: NCT05091073
• Lead Sponsor: Novo Nordisk A/S

Brief Summary

In this study participants will receive NNC0385-0434. NNC0385-0434 is being developed for the treatment of hypercholesterolemia, a fat metabolism disorder characterized by high levels of cholesterol in the blood. The dose to be tested in this study is 40 mg NNC0385-0434.

NNC0385-0434 is a new potential medicine that is currently being tested for intake as a tablet. It is not yet approved and cannot be prescribed yet. Besides 40 mg of NNC0385-0434, each tablet also contains 500 mg of the absorption enhancing agent SNAC, which helps to move NNC0385-0434 from the stomach into the blood.

The aim of this study is to investigate the effect of food intake on the amount of NNC0385-0434 in the blood after multiple tablet intake. For this purpose, NNC0385-0434 is given either after a high-fat breakfast or on an empty stomach. After dosing, participants must either fast for another 4 hours or receive a meal 30 minutes after dosing, depending on the group participants are assigned to. After taking the NNC0385-0434 tablets, the amount of NNC0385-0434 (and of SNAC) in the blood will be measured. The effect of food intake on the uptake of NNC0385-0434 into the body will be investigated so that correct and safe intake recommendations and medicine labels can be given.

The study can last for up to approximately 14 weeks for each participant, with a total of 7 clinic visits. This includes a screening period (up to 4 weeks) and one in-house treatment period (together a total of 13 consecutive days). It also includes a follow-up period with 5 ambulatory visits at the clinic (for approximately 7 weeks \[total of 50 days\] after the last dosing). participants will have blood tests at every clinic visit. Participants must be healthy and have a body mass index (BMI) between 20.0 and 34.9 kg/m2 (both inclusive). Only men can participate in this clinical study.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2021-10-22
• Study First Submitted QC: 2021-10-22
• Study First Posted: 2021-10-25
• Study Start: 2021-12-09
• Primary Completion: 2022-04-07
• Study Completion: 2022-05-31
• Status Verified: 2023-12
• Last Update Submitted: 2023-12-22
• Last Update Posted: 2023-12-26

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 73

Inclusion Criteria

• Male.
• Aged 18 to 55 (both inclusive).
• Considered to be generally healthy based on medical history, physical examination, and the results of vital signs, ECG and clinical laboratory tests performed during the screening visit, as judged by the investigator.
• Body weight minimum 54 kg.
• Body mass index (BMI) between 20.0 and 34.9 kg/m^2 (both inclusive).

Exclusion Criteria

• Any disorder, which in the investigator's opinion might jeopardise participant safety or compliance with the protocol.
• Meal habits and diet requirements which are contradictory to the meals provided or unwillingness to eat the food provided in the study.
• Presence of clinically significant gastrointestinal disorders potentially affecting absorption of drugs and/or nutrients, as judged by the investigator.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Reference group	NNC0385-0434	Reference dosing conditions
Fasting group	NNC0385-0434	Fasting dosing conditions
Fed group	NNC0385-0434	Fed dosing conditions

Primary Outcome Measures

Name	Time	Method
AUC0-24h,0434,Day10: the area under the NNC0385-0434 plasma concentration-time curve from 0 to 24 h after last dose of oral NNC0385-0434	From last dose (Day 10) to 24 hours post treatment (Day 11)	h\*nmol/L

Secondary Outcome Measures

Name	Time	Method
Cmax,0434,Day10: the maximum plasma concentration of NNC0385-0434 after last dose of oral NNC0385-0434	From last dose (Day 10) to post treatment follow-up (Day 65)	nmol/L
t1/2,0434,Day10: the terminal half-life of NNC0385-0434 after last dose of oral NNC0385-0434	From last dose (Day 10) to post treatment follow-up (Day 65)	hours
tmax,0434,Day10: the time to maximum observed plasma concentration of NNC0385-0434 after last dose of NNC0385-0434	From last dose (Day 10) to post treatment follow-up (Day 65)	hours

Trial Locations

Locations (1)

Novo Nordisk Investigational Site; 🇩🇪 Berlin, Germany