Last reviewed · How we verify

NCT07076030

Pharmacokinetics of Petrelintide Following Administration to Participants With Impaired Renal Function

Completed Phase 1 Last updated 28 January 2026
What this trial tests

Phase 1 trial testing Petrelintide in Renal Impairment in 39 participants. Completed in 25 November 2025.

Timeline
15 April 2025
Primary endpoint
25 November 2025
25 November 2025

Quick facts

Lead sponsorZealand Pharma
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment39
Start date15 April 2025
Primary completion25 November 2025
Estimated completion25 November 2025
Sites1 location across Germany

Drugs / interventions tested

Conditions studied

Sponsor

Zealand Pharma — full company profile →

Who can join

Adults 18 to 65, any sex, with Renal Impairment. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This clinical research study is testing the study compound petrelintide that is being developed for the weight management in people with obesity or overweight with comorbidities or related diseases. The aim of this clinical research study is to investigate whether the effects of petrelintide will be different in people with normal kidney function compared to people with impaired kidney function.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Petrelintide

Trials testing the same drug.

Other recruiting trials for Renal Impairment

Currently open trials in the same condition.

Other Zealand Pharma trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07076030.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing