The purpose of the study is to assess the safety, tolerability, antiviral effects, and pharmacokinetics of PPI-461 in patients with chronic hepatitis C virus genotype 1 infection.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
24
Local Institution
Sacramento, California, United States
Local institution
San Francisco, California, United States
Local institution
Aarhus, Denmark
Local institution
Copenhagen, Denmark
Safety and tolerability, as measured by clinical adverse events and laboratory assessments
Time frame: up to Study Day 16 (14 days after the last PPI-461 dose)
Antiviral effects of PPI-461, as measured by HCV RNA levels
Time frame: Up to Study Day 16 (14 days after the last PPI-461 dose)
PPI-461 pharmacokinetics as measured by plasma PPI-461 concentrations
Time frame: Up to Study Day 10 (8 days after the last PPI-461 dose)
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Local institution
Herlev, Denmark
Local institution
Hvidovre, Denmark
Local institution
Kolding, Denmark
Local institution
Odense, Denmark
Local institution
London, United Kingdom
Local institution
London, United Kingdom
...and 1 more locations