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Experimental: Valacyclovir treatment

University of Pittsburgh · FDA-approved active Small molecule

Experimental: Valacyclovir treatment is a Nucleoside analog antiviral Small molecule drug developed by University of Pittsburgh. It is currently FDA-approved for Herpes simplex virus (HSV-1 and HSV-2) infection, Varicella-zoster virus (chickenpox and shingles) infection, Cytomegalovirus (CMV) infection prophylaxis in immunocompromised patients.

Valacyclovir is a prodrug that is converted to acyclovir, which inhibits viral DNA polymerase to prevent herpesvirus replication.

Valacyclovir is a prodrug that is converted to acyclovir, which inhibits viral DNA polymerase to prevent herpesvirus replication. Used for Herpes simplex virus (HSV-1 and HSV-2) infection, Varicella-zoster virus (chickenpox and shingles) infection, Cytomegalovirus (CMV) infection prophylaxis in immunocompromised patients.

At a glance

Generic nameExperimental: Valacyclovir treatment
SponsorUniversity of Pittsburgh
Drug classNucleoside analog antiviral
TargetHerpesvirus DNA polymerase
ModalitySmall molecule
Therapeutic areaInfectious Disease / Virology
PhaseFDA-approved

Mechanism of action

Valacyclovir is rapidly metabolized to acyclovir in the body. Acyclovir is phosphorylated by viral thymidine kinase in infected cells, then further phosphorylated to the active triphosphate form, which competitively inhibits viral DNA polymerase and causes chain termination of viral DNA synthesis. This mechanism is selective for herpesvirus-infected cells.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

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Frequently asked questions about Experimental: Valacyclovir treatment

What is Experimental: Valacyclovir treatment?

Experimental: Valacyclovir treatment is a Nucleoside analog antiviral drug developed by University of Pittsburgh, indicated for Herpes simplex virus (HSV-1 and HSV-2) infection, Varicella-zoster virus (chickenpox and shingles) infection, Cytomegalovirus (CMV) infection prophylaxis in immunocompromised patients.

How does Experimental: Valacyclovir treatment work?

Valacyclovir is a prodrug that is converted to acyclovir, which inhibits viral DNA polymerase to prevent herpesvirus replication.

What is Experimental: Valacyclovir treatment used for?

Experimental: Valacyclovir treatment is indicated for Herpes simplex virus (HSV-1 and HSV-2) infection, Varicella-zoster virus (chickenpox and shingles) infection, Cytomegalovirus (CMV) infection prophylaxis in immunocompromised patients.

Who makes Experimental: Valacyclovir treatment?

Experimental: Valacyclovir treatment is developed and marketed by University of Pittsburgh (see full University of Pittsburgh pipeline at /company/university-of-pittsburgh).

What drug class is Experimental: Valacyclovir treatment in?

Experimental: Valacyclovir treatment belongs to the Nucleoside analog antiviral class. See all Nucleoside analog antiviral drugs at /class/nucleoside-analog-antiviral.

What development phase is Experimental: Valacyclovir treatment in?

Experimental: Valacyclovir treatment is FDA-approved (marketed).

What are the side effects of Experimental: Valacyclovir treatment?

Common side effects of Experimental: Valacyclovir treatment include Headache, Nausea, Abdominal pain, Diarrhea, Tremor (at high doses), Confusion or hallucinations (rare, high-dose).

What does Experimental: Valacyclovir treatment target?

Experimental: Valacyclovir treatment targets Herpesvirus DNA polymerase and is a Nucleoside analog antiviral.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing