150
Participants
Start Date
June 1, 2026
Primary Completion Date
June 1, 2028
Study Completion Date
June 1, 2029
Acyclovir 50 MG/ML
Patients are randomised to active treatment with IV acyclovir with the possibility of step-down to valacyclovir. If the treating physician prefers, initial IV treatment can be omitted and the patient can be treated with valacyclovir throughout the study period.
Placebo
Placebo either in IV formulation or as tablets identical to valacyclovir tablets.
Jacob Bodilsen
OTHER