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Prednisolone + valaciclovir

Uppsala University Hospital · FDA-approved active Small molecule

Prednisolone suppresses immune and inflammatory responses while valaciclovir inhibits viral DNA replication, together reducing inflammation and controlling herpes virus infection.

Prednisolone suppresses immune and inflammatory responses while valaciclovir inhibits viral DNA replication, together reducing inflammation and controlling herpes virus infection. Used for Herpes zoster (shingles) with inflammatory complications, Bell's palsy associated with herpes simplex virus.

At a glance

Generic namePrednisolone + valaciclovir
SponsorUppsala University Hospital
Drug classCorticosteroid + antiviral combination
TargetGlucocorticoid receptor (prednisolone); herpes simplex virus and varicella-zoster virus DNA polymerase (valaciclovir)
ModalitySmall molecule
Therapeutic areaImmunology / Infectious Disease
PhaseFDA-approved

Mechanism of action

Prednisolone is a corticosteroid that decreases immune cell activity and inflammatory mediator production. Valaciclovir is a prodrug of acyclovir that inhibits herpes simplex virus and varicella-zoster virus DNA polymerase, preventing viral replication. The combination addresses both the inflammatory and infectious components of certain viral conditions.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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