Current Study: PH1

Purpose:
• To determine how the investigational drug is broken down and removed from the body in volunteers with liver impairment when compared to volunteers with normal liver function.
• Information regarding safety and side effects that may occur will also be collected
• This study is for research purposes only and is not intended to treat your liver disease.

Method of Administration: Single oral dose of study medication

Investigator: Thomas Marbury, MD

To qualify:

• 18 to 65 years old
• Must have decreased liver function or disease such as fatty liver disease, Hepatitis C, or past history of alcohol related liver disease
• Volunteers may be taking medicines such as spironolactone, Lasix®, lactulose, Aldactone®, or rifaximin
• May also have fluid in your abdomen, cirrhosis, or encephalopathy (brain condition that causes irritability or trouble sleeping

Length/Duration
• 4 days and 3 nights in our research facility

Location 5055 South Orange Avenue, Orlando, FL 32809

Compensation
Qualified participants will receive study medication, study related physical exams and laboratory tests

Qualified study participants will be compensated up to $1,650 for time and travel

Whom to Contact Recruitment Department: 407-240-7876