A Research Study Looking Into Blood Levels of the Medicine NNC0487-0111 in the Body and How Well it is Tolerated in People With Reduced Liver Function and Normal Liver Function
Overweight · Obesity
What this study involves
The registry says this study is recruiting. Individual locations may have different availability.
- Study type
- Interventional
- Phase
- Phase 1
- Age range
- 18 years - 80 years
- Sex eligible
- All sexes
- Healthy volunteers
- Not accepted
- Participants
- 35 Estimated
These are starting points, not an eligibility decision. The research team must review the full requirements.
About the research
The study is testing a new study medicine to treat people with overweight/obesity and type 2 diabetes. The aim of this study is to see if it is safe and to find out how it works in people with reduced liver function and people with normal liver function.
Who may be able to participate?
The list below is the sponsor’s full registry wording. It can include conditions, prior treatment, test results and other requirements. A match in search does not mean you qualify.
Inclusion Criteria:
- Male or female (sex at birth).
- Age 18-80 years (both inclusive) at the time of signing informed consent.
- 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.
Treatment, groups and participation
The registry may describe treatments and study duration without a complete visit calendar. Ask the study team for the exact schedule, procedures, risks, costs and alternatives. Keep your usual care plan unless your treating clinician tells you otherwise.
- Assignment
- Not randomized
- Masking
- No masking
Severe hepatic impairment
Participants will receive single dose of NNC0487-0111 subcutaneously.
Drug: NNC0487-0111
Moderate hepatic impairment
Participants will receive single dose of NNC0487-0111 subcutaneously.
Drug: NNC0487-0111
Mild hepatic impairment
Participants will receive single dose of NNC0487-0111 subcutaneously.
Drug: NNC0487-0111
Normal hepatic impairment
Participants will receive single dose of NNC0487-0111 subcutaneously.
Drug: NNC0487-0111
NNC0487-0111 DRUG
NNC0487-0111 will be administered subcutaneously using PDS290 pre-filled pen-injectors in a skinfold in the thigh.
What researchers are measuring
Outcome measures describe what is being studied. They are not proof that a treatment works.
Primary measures
AUC0-∞: The area under the NNC0487-0111 plasma concentration-time curve from time 0 to infinity after a single dose
Time frame: From pre-dose on Day 1 up to Day 28
Measured as hours\*nanomole per liter (nmol\*h/L)
Secondary measures
Cmax: Maximum observed plasma NNC0487-0111 concentration after a single dose
Time frame: From pre-dose on Day 1 until Day 5
Measured as nanomoles per liter (nmol/L)
tmax: Time to maximum observed plasma NNC0487-0111 concentration after a single dose
Time frame: From pre-dose on Day 1 until Day 5
Measured as hour
t½,: Terminal half-life for NNC0487-0111 after a single dose
Time frame: From pre-dose on Day 1 up to Day 28
Measured as hour
Vz/F: Apparent volume of distribution of NNC0487-0111 after a single dose
Time frame: From pre-dose on Day 1 up to Day 28
Liter
CL/F: Apparent clearance of NNC0487-0111 after a single dose
Time frame: From pre-dose on Day 1 up to Day 28
Measured as liter per hour (L/h)
Number of treatment emergent adverse events (TEAEs)
Time frame: From pre-dose on Day 1 up to Day 28
Measured as number of events
Review the complete result tables and limitations in the official record.
Open official results ↗Research locations (2)
The overall study status and a local site’s status can differ. Confirm that location’s availability before traveling.
2 locations
Summit Clinical Research s.r.o.Bratislava, SlovakiaRecruiting
Summit Clinical Research s.r.o.Malacky, SlovakiaRecruiting
Study team and timeline
- Lead sponsor
- Novo Nordisk A/S
- Study start
- May 13, 2026 Actual
- Primary completion
- Dec 1, 2027 Estimated
- Study completion
- Dec 1, 2027 Estimated
- First posted
- May 14, 2026 Actual
- Last updated
- Nov 10, 2026 Actual
Official study contacts
Official study title
A Study Investigating the Pharmacokinetic Properties, Safety and Tolerability of NNC0487-0111 in Participants With Various Degrees of Hepatic Impairment and Participants With Normal Hepatic Function
Ask Wellness Clinical Research
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Source: ClinicalTrials.gov API v2. Information is submitted by sponsors and investigators. NLM does not approve the safety or science of all listed studies. Registry disclaimer.
Retrieved: Nov 12, 2026 · Last registry update: Nov 10, 2026
