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Pharmacokinetics of Anacetrapib (MK0859) in Patients With Hepatic Insufficiency (MK-0859-039)

A Single Dose Study to Investigate the Pharmacokinetics of MK0859 in Patients With Hepatic Insufficiency

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01114490
Enrollment
24
Registered
2010-05-03
Start date
2010-05-31
Completion date
2010-07-31
Last updated
2015-10-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dyslipidemia

Keywords

Hepatic Insufficiency

Brief summary

This study will evaluate the Area Under the Curve (AUC(0 to infinity)) of anacetrapib.

Interventions

single dose administration of anacetrapib (MK0859) 100 mg oral tablet

Sponsors

Merck Sharp & Dohme LLC
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Female subjects of reproductive potential test negative for pregnancy and agree to use two acceptable methods of birth control throughout the study * Subject is in good health * Subject agrees to refrain from consumption of red wine, grapefruit, orange and apple juices throughout the study

Exclusion criteria

* Patient has a history of cancer * Patient is a nursing mother * Patient is unable to refrain from or anticipates the use of any prescription or non-prescription medication during the study * Patient consumes excessive amounts of alcohol or caffeine * Patient has had major surgery, donated blood or participated in another investigational study within the past 4 weeks

Design outcomes

Primary

MeasureTime frame
Area Under the Curve (AUC(0 to infinity)) of anacetrapibthrough 168 hours post dose

Secondary

MeasureTime frame
Tolerability of a single dose administration of 100mg anacetrapib, measured by the number of clinical and laboratory adverse eventsthrough 14 days post dose

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026