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Cidofovir intravenous

Johns Hopkins Bloomberg School of Public Health · Phase 3 active Small molecule

Cidofovir is a nucleotide analog that inhibits viral DNA polymerase, preventing viral DNA replication in infected cells.

Cidofovir is a nucleotide analog that inhibits viral DNA polymerase, preventing viral DNA replication in infected cells. Used for Cytomegalovirus (CMV) retinitis in immunocompromised patients, CMV and other viral infections in immunocompromised populations.

At a glance

Generic nameCidofovir intravenous
Also known asVistide
SponsorJohns Hopkins Bloomberg School of Public Health
Drug classNucleotide analog antiviral
TargetViral DNA polymerase
ModalitySmall molecule
Therapeutic areaInfectious Disease / Virology
PhasePhase 3

Mechanism of action

Cidofovir is a cytosine nucleotide analog that is phosphorylated intracellularly and then incorporated into viral DNA, causing chain termination and inhibiting viral DNA polymerase. It has broad-spectrum activity against DNA viruses including cytomegalovirus (CMV), herpesviruses, and other viral pathogens. The drug is particularly useful for treating infections in immunocompromised patients where conventional antivirals may be ineffective or resistance has developed.

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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