PK and Safety in Participants Taking Obicetrapib With Moderate Hepatic Impairment Relative to Normal Hepatic Function
NCT06048302 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 18
Last updated 2024-09-19
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).
Conditions
- Hepatic Impairment
- Healthy
Interventions
- DRUG
-
Obicetrapib
1 single dose of obicetrapib
Sponsors & Collaborators
-
Veranex
collaborator UNKNOWN -
NewAmsterdam Pharma
lead INDUSTRY
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- OTHER
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-11-30
- Primary Completion
- 2024-03-12
- Completion
- 2024-03-19
- FDA Drug
- Yes
Countries
- United States
Study Locations
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