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Relenza (ZANAMIVIR)

GSK · FDA-approved approved Small molecule Verified Quality 70/100

Relenza works by blocking the neuraminidase enzyme, preventing the influenza virus from spreading and infecting new cells.

Relenza (ZANAMIVIR) is a small molecule neuraminidase inhibitor developed by Glaxosmithkline, targeting Sialidase 3 to treat influenza. It was FDA approved in 1999 and remains a branded product due to its off-patent status. Despite low bioavailability of 2%, its short half-life of 1.7 hours allows for effective treatment. Relenza is used to treat influenza, but its commercial status as an off-patent product limits its availability. Key safety considerations include its potential to cause respiratory issues and its inhaled administration method.

At a glance

Generic nameZANAMIVIR
SponsorGSK
Drug classNeuraminidase Inhibitor [EPC]
TargetSialidase 3
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved
First approval1999

Mechanism of action

Zanamivir is an antiviral drug with activity against influenza virus [see Microbiology (12.4)].

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

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