Overview

PK and Safety in Participants Taking Obicetrapib With Moderate Hepatic Impairment Relative to Normal Hepatic Function

Status:
Recruiting
Trial end date:
2024-07-30
Target enrollment:
Participant gender:
Summary
To investigate the safety and pharmacokinetics in patients with moderate hepatic impairment compared to healthy participants after a single oral dose of obicetrapib (10 mg).
Phase:
Phase 1
Details
Lead Sponsor:
NewAmsterdam Pharma
Collaborator:
Veranex