Hepatic Impairment Study
Completed · Phase 1
Conditions studied: Liver Disease
In brief
This study is to find out how the subject's body processes and reacts to the study drug, and to find out how long it remains in the subjects system after one dose. Subjects with varying degrees of liver function are being asked to participate in this study. Study results from subjects with normal liver function will be compared with study results from subjects with impaired liver function.
Key facts
- Study ID
- NCT00829231
- Run by
- Bayer
- People needed
- 45
- Starts
- 2009-01-01
- Expected to finish
- 2009-07-01
- Last updated by the study team
- 2014-11-03
Who can join
Age: 50 and older, up to 75. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy Subjects, Child Pugh A and Child Pugh B Liver Disease Patients.
Where it is running
- Study site — Miami, Florida, United States
- Study site — Orlando, Florida, United States
- Study site — Knoxville, Tennessee, United States
Full record on ClinicalTrials.gov
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