This is a Phase 1 study of imiquimod, a new immunomodulator that has demonstrated antiviral activity. The primary objective is to assess the safety and tolerance of imiquimod administered over an 8 week period to ambulatory outpatients with chronic hepatitis C and histologic proven chronic active hepatitis with or without cirrhosis. A secondary objective is to obtain data on interferon and other cytokine induction, along with pharmacokinetic data on imiquimod.

Project Start
Project End
Budget Start
Budget End
Support Year
36
Fiscal Year
1996
Total Cost
Indirect Cost
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