This non-randomized, multi-center, open-label study will evaluate the pharmacokinetics and the safety and tolerability of danoprevir (RO5190591) and ritonavir in healthy volunteers and patients with mild, moderate or severe hepatic impairment. Participants will be administered repeated daily doses of danoprevir and ritonavir. The anticipated time on study treatment is 10 days.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
81
Repeated oral doses
Repeated oral doses
Unnamed facility
Lenexa, Kansas, United States
Unnamed facility
Prague, Czechia
Unnamed facility
Prague, Czechia
Unnamed facility
Bratislava, Slovakia
Unnamed facility
Bratislava, Slovakia
Pharmacokinetics (plasma concentration) of danoprevir in patients with hepatic impairment
Time frame: From baseline to day 10
Safety and tolerability (incidence of adverse events) of danoprevir in patients with hepatic impairment
Time frame: From baseline to day 10
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