This study is designed to test the hypothesis that African-Americans respond less well to combination pegylated interferon and ribavirin therapy than Caucasian-Americans who have chronic hepatitis C genotype 1 and who were not previously treated with either interferon or ribavirin. Reasons for differences in response, regardless of race, will be studied.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
401
University of California, San Francisco
San Francisco, California, United States
University of Miami School of Medicine
Miami, Florida, United States
Rush University
Chicago, Illinois, United States
University of Maryland School of Medicine
Sustained Virologic Response (SVR)
The primary end point of therapy was an SVR that was definied as the absences of detectable HCV RNA in serum 24 weeks after therapy was stopped.
Time frame: 24 weeks after therapy is discontinued
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Baltimore, Maryland, United States
Beth Israel Deaconess Medical Center
Boston, Massachusetts, United States
University of Michigan Medical Center
Ann Arbor, Michigan, United States
New York-Presbyterian Medical Center
New York, New York, United States
University of North Carolina
Chapel Hill, North Carolina, United States