To investigate the efficacy and safety of three different doses of ASP2151, as compared to valacyclovir hydrochloride in subjects with herpes zoster, and to determine the recommended clinical dose.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
403
oral
oral
Unnamed facility
Chūbu, Japan
Unnamed facility
Hokkaido, Japan
Unnamed facility
Kanto, Japan
Unnamed facility
Kinki, Japan
Unnamed facility
Kyusyu, Japan
To compare the efficacy and safety of ASP2151 with valacyclovir in subjects with Herpes Zoster
Time frame: 3 months
Improvement of cutaneous symptoms and pain
Time frame: 3 months
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