This proof of concept study is designed to evaluate the safety, tolerability, pharmacokinetics, and antiviral activity of TD-6450 in treatment naïve subjects with GT-1, GT-2 or GT-3 chronic HCV.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
47
Texas Liver Institute
San Antonio, Texas, United States
Adverse events
Number, type, severity, and association of treatment emergent adverse events.
Time frame: 28 Days
Cmax
Cmax
Time frame: 28 Days
Tmax
Tmax
Time frame: 28 Days
AUC0-t
Time frame: 28 Days
AUC0-∞
AUC0-∞
Time frame: 28 Days
AUC0-24
Time frame: 28 Days
Antiviral Activity
Change from baseline in HCV RNA
Time frame: 28 Days
t1/2
t1/2
Time frame: 28 Days
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