A Research Study Looking at How a Single Dose of the Study Medicine NNC0194-0499 Behaves in Participants With Reduced Liver Function Compared to Participants With Normal Liver Function

Phase 1

Completed

• Conditions: Healthy Volunteers; Hepatic Impairment
• Interventions: Drug: NNC0194-0499

• Registration Number: NCT05917938
• Lead Sponsor: Novo Nordisk A/S

Brief Summary

The study medicine NNC0194-0499 is under development for non-alcoholic fatty liver disease (NAFLD) including non-alcoholic steatohepatitis (NASH). All participants will receive a single dose of 30 milligram (mg) of the study medicine. The study medicine will be given in the form of an injection of 0.6 millilitres in a skinfold of the thigh (subcutaneous). The study will last for up to 64 days. Women cannot take part if pregnant, breast-feeding or plan to get pregnant during the study period. Women who are able to become pregnant must use highly effective contraception and will be counselled on the use of contraception. Participants with impaired liver function will undergo an ultrasound of the belly and measurement of brain activity.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2023-06-08
• Study First Submitted QC: 2023-06-23
• Study First Posted: 2023-06-26
• Study Start: 2023-07-04
• Primary Completion: 2024-12-16
• Study Completion: 2024-12-16
• Status Verified: 2025-02
• Last Update Submitted: 2025-02-21
• Last Update Posted: 2025-02-24

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 33

Inclusion Criteria

• Male or female.
• Aged 18-80 years (both inclusive) at the time of signing informed consent.
• Body mass index (BMI) between 18.5-39.9 kilogram per square meter (kg/m^2) (both inclusive). Specific inclusion criterion only for participants with hepatic impairment:
• Participants with stable hepatic impairment classified as Child-Pugh grade A, B or C as assessed by the investigator. Stable hepatic impairment is defined as no clinically significant change in disease status, as judged by the investigator.

Exclusion Criteria

• Known or suspected hypersensitivity to study intervention(s) or related products.
• Female who is pregnant, breast-feeding or intends to become pregnant or is of child-bearing potential and not using a highly effective contraceptive method.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Participants With Moderate Hepatic Impairment	NNC0194-0499	Participants with moderate hepatic impairment (Child-Pugh Grade B) will receive a single subcutaneous dose of 30 mg of NNC0194-0499 on Day 1.
Participants With Severe Hepatic Impairment	NNC0194-0499	Participants with severe hepatic impairment (Child-Pugh Grade C) will receive a single subcutaneous dose of 30 mg of NNC0194-0499 on Day 1.
Participants With Mild Hepatic Impairment	NNC0194-0499	Participants with mild hepatic impairment (Child Pugh Grade A) will receive a single subcutaneous dose of 30 mg of NNC0194-0499 on Day 1.
Participants With Normal Hepatic Function	NNC0194-0499	Participants with normal hepatic function will receive a single subcutaneous dose of 30 milligram (mg) of NNC0194-0499 on Day 1.

Primary Outcome Measures

Name	Time	Method
AUC0-∞, Single Dose, NNC0194-0499: the area under the NNC0194-0499 serum concentration-time curve from time 0 to infinity after a single dose	From 0 hours (Day 1) until end of study visit (Day 36)	Measured in nanomoles hour per liter (nmol h/L).

Secondary Outcome Measures

Name	Time	Method
Cmax, NNC0194-0499: the maximum concentration of NNC0194-0499 in serum	From Day 1 (pre-dose) until completion of the post-treatment follow-up visit (Day 36)	Measured in nanomoles per liter (nmol/L).
Number of treatment emergent adverse events (TEAEs)	From time of trial product administration (Visit 2, Day 1) until completion of the end of trial visit (Visit 8, Day 36)	Measured as number of events.
tmax, NNC0194-0499: the time from dose administration to maximum serum concentration of NNC0194-0499	From Day 1 (pre-dose) until completion of the post-treatment follow-up visit (Day 36)	Measured in hours.
Vz/F, NNC0194-0499: apparent volume of distribution of NNC0194-0499 after a single dose	From Day 1 (pre-dose) until completion of the end of trial visit (Day 36)	Measured in liters.
t1/2, NNC0194-0499: the terminal half-life of NNC0194-0499 in serum	From Day 1 (pre-dose) until completion of the post-treatment follow-up visit (Day 36)	Measured in hours.
CL/F, NNC0194-0499: the apparent total serum clearance of NNC0194-0499	From Day 1 (pre-dose) until completion of the post-treatment follow-up visit (Day 36)	Measured in liters per hour.

Trial Locations

Locations (3)

Uniwersyteckie Centrum Kliniczne (UCK); 🇵🇱 Gdańsk, Poland

Summit Clinical Research s.r.o.; 🇸🇰 Malacky, Slovakia

APEX Research; 🇩🇪 München, Germany