The aim of this study is therefore to investigate the efficacy of the PEG-formulation to reduce the frequency and duration of genital herpes recurrences, to assess its safety and tolerability and to investigate its effect on shedding.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
8
University Hospital Zurich
Zurich, Canton of Zurich, Switzerland
Change of number of genital herpes recurrences during the treatment period as compared to the baseline period.
The number of genital herpes recurrences will be counted during the baseline period (6 months) and during the treatment period (6 months) and then be compared.
Time frame: Baseline and Treatment period (6 months each).
The safety of the PEG-formulation via reporting of AEs.
Time frame: Baseline and Treatment period (6 months each).
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