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

NCT05091073 | Completed Phase 1

• 3 other identifiers: NN6435-4826U1111-1264-46932021-000430-34
• Study Type: interventional
• Target: 73
• Locations: 1 country
• Sites: 1

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.

Conditions

Established Atherosclerotic Cardiovascular Disease (ASCVD) or ASCVD Risk; Elevated Cholesterol; Healthy Volunteers

Outcome Measures

Primary Outcomes (1)

• 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

  h\*nmol/L

  From last dose (Day 10) to 24 hours post treatment (Day 11)

Secondary Outcomes (3)

• 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)

• 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)

• 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)

Study Arms (3)

Fed group

EXPERIMENTAL

Fed dosing conditions

Drug: NNC0385-0434

Fasting group

EXPERIMENTAL

Fasting dosing conditions

Drug: NNC0385-0434

Reference group

ACTIVE COMPARATOR

Reference dosing conditions

Drug: NNC0385-0434

Interventions

NNC0385-0434 DRUG

All participants will be dosed with 40 mg oral NNC0385-0434 once-daily for 10 consecutive days

Fasting group; Fed group; Reference group

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: male
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• 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).

You may not qualify if:

• 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.

Sponsors & Collaborators

• Novo Nordisk A/S: lead

Study Sites (1)

Novo Nordisk Investigational Site

Berlin, 14050, Germany

Location

MeSH Terms

Conditions

Hypercholesterolemia

Condition Hierarchy (Ancestors)

Hyperlipidemias; Dyslipidemias; Lipid Metabolism Disorders; Metabolic Diseases; Nutritional and Metabolic Diseases

Study Officials

• Clinical Transparency (dept. 2834)

  Novo Nordisk A/S

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 22, 2021
• First Posted: October 25, 2021
• Study Start: December 9, 2021
• Primary Completion: April 7, 2022
• Study Completion: May 31, 2022
• Last Updated: December 26, 2023

Record last verified: 2023-12

Data Sharing

• IPD Sharing: Will share

Locations

DE (1)