Pharmacokinetics of Petrelintide in Participants With Impaired Hepatic Function
Recruiting now · Phase 1
Conditions studied: Impaired Hepatic Function
In brief
This clinical research trial is testing the investigational medicinal product (IMP) petrelintide that is being developed for body weight reduction in people living with obesity or overweight who have comorbidities. The aim of this clinical research trial is to investigate whether the pharmacokinetics (PK) of petrelintide will be different in people with hepatic impairment (HI) compared to people with normal hepatic function.
Key facts
- Study ID
- NCT07682818
- Run by
- Zealand Pharma
- People needed
- 36
- Starts
- 2026-05-18
- Expected to finish
- 2027-04-12
- Last updated by the study team
- 2026-07-06
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- All participants:
- Sex: male and female participants.
- Body mass index (BMI): 18.5 to 40.0 kg/m\^2, inclusive, at screening.
- Additional Inclusion Criteria for Participants with Normal Hepatic Function
- Participants who are considered healthy as determined by medical history, physical examination, and other screening procedures, with clinically normal hepatic function at screening..
- Clinical laboratory test results within normal reference range for the population, or results with acceptable deviations that are judged not to be clinically significant by the Investigator.
- Additional Inclusion Criteria for Participants with Hepatic Impairment
- Participants with stable HI for at least 3 months, classified as Child-Pugh Grade A, B, or C as assessed by the Investigator.
- Participants should be otherwise judged to be in acceptable health (type 2 diabetes mellitus [T2DM] is allowed) in the opinion of the Investigator based on a medical evaluation (including a physical examination, medical history, electrocardiogram [ECG], vital signs, concomitant medication and the results of laboratory safety tests) performed during the screening visit.
- Participants with T2DM may be enrolled if they have/are: a. Hemoglobin A1c ≤11% at screening b. On a stable regimen for at least 8 weeks prior to screening, defined as: stable diet and exercise program, and/or, stable dose of metformin, and/or, stable dose of a sodium-glucose cotransporter-2 inhibitor.
You may not qualify if…
- All participants:
- Known or suspected hypersensitivity to the IMP 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.
Where it is running
- Centrum Badan Klinicznych Piotr Napora Lekarze sp.p. — Wroclaw, Poland, Poland (enrolling)
- Summit Clinical Research s.r.o. — Bratislava, Bratislava Region, Slovakia (enrolling)
- Summit Clinical Research s.r.o. — Malacky, Malacky, Slovakia (enrolling)
Full record on ClinicalTrials.gov
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