The Influence of Hepatic Insufficiency on the Pharmacokinetics of Elbasvir (MK-8742) (MK-8742-009)

Completed · Phase 1

Conditions studied: Hepatic Insufficiency

In brief

The purpose of this study is to evaluate the pharmacokinetics (PK) profile of elbasvir (MK-8742) after a single dose to participants with mild, moderate, or severe hepatic insufficiency compared with healthy controls.

Key facts

Study ID

NCT01797536

Run by

Merck Sharp & Dohme LLC

People needed

31

Starts

2013-03-06

Expected to finish

2014-08-20

Last updated by the study team

2018-10-25

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Body mass index (BMI) 19 - 40 kg/m\^2, inclusive
• In good health based on medical history, physical examination, vital signs, and laboratory safety tests
• No clinically significant abnormality on electrocardiogram (ECG)
• For participants with hepatic insufficiency only, diagnosis of chronic (> 6 months), stable (no acute episodes of illness within the previous 2 months due to deterioration in hepatic function) hepatic insufficiency with features of cirrhosis due to any cause
• For participants with hepatic insufficiency only, score on the Child-Pugh scale must range from 5 to 6 for mild hepatic insufficiency, from 7 to 9 for moderate hepatic insufficiency, and from 10 to 15 for severe hepatic insufficiency
• Females of childbearing potential must be either be sexually inactive (abstinent) for 14 days before study drug administration and throughout the study or be using an acceptable method of birth control
• Females of non-childbearing potential must have undergone sterilization procedures at least 6 months before Study Day 1
• Non-vasectomized males must agree to use a condom with spermicide or abstain from sexual intercourse during the study and for 3 months after study drug administration
• Ability to swallow multiple capsules

You may not qualify if…

• Previously enrolled in this study
• Mentally or legally incapacitated, significant emotional problems at the time of screening or expected during the conduct of the study, or a history of a clinically significant psychiatric disorder over the last 5 years
• History or presence of significant cardiovascular, pulmonary, renal, hematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurological disease
• History of any illness that might confound the results of the study or pose an additional risk to the participant by participating in the study
• For participants with hepatic insufficiency only, estimated creatinine clearance (CrCl) ≤30 mL/min based on the Cockcroft-Gault equation at screening
• History or presence of drug abuse within the past 2 years
• For healthy participants only, history of alcoholism within the past 2 years
• Females who are pregnant or lactating
• Positive results for the urine drug screen at screening or check-in
• Positive results at screening or history of human immunodeficiency virus (HIV) or untreated hepatitis C virus (HCV); HCV ribonucleic acid (RNA)-negative participants documented to be cured following anti-HCV treatment are eligible
• For healthy participants only, positive results at screening for hepatitis B surface antigen (HBsAg)
• Use of any drugs or substances known to be strong inhibitors of cytochrome P450 3A4 (CYP3A4) enzymes and/or P-glycoprotein (P-gp) or any inhibitors of organic anion transporting peptide 1B (OATP1B) within 14 days or 5-times the half-life of the product (for healthy participants) or which cannot be discontinued at least 14 days or 5 times the half-life of the product (for hepatic insufficiency participants) before study drug administration and throughout the study
• Use of any drugs or substances known to be strong inducers of CYP3A4 enzymes and/or P-gp, including St-John's Wort or rifampin, within 28 days or 5 times the half-life of the product before study drug administration
• Currently use of any medication or substance which cannot be discontinued or maintained at a steady dose and regimen at least 14 days before study drug administration and throughout the study
• For healthy participants only, on a special diet within 28 days before study drug administration
• Blood donation >500 mL or significant blood loss within 56 days before study drug administration
• Plasma donation within 7 days before study drug administration
• Participation in another clinical study within 28 days before study drug administration

Where it is running

• Call for Information (Investigational Site 0003) — Miami, Florida, United States
• Call for Information (Investigational Site 0001) — Orlando, Florida, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.