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Pfizer launches large study of oral COVID-19 prevention drug

Click to play video: 'U.S. FDA, CDC support Pfizer-BioNTech boosters for people high-risk or aged 65+'
U.S. FDA, CDC support Pfizer-BioNTech boosters for people high-risk or aged 65+
The U.S. Food and Drug Administration (FDA) and an advisory panel for the Centers for Disease Control and Prevention say Americans aged 65 years and older, and those who have a high risk for severe disease should receive a third dose of the Pfizer-BioNTech COVID-19 vaccine. Jackson Proskow reports on if Canada is looking to follow suit, and how scientists feel about the general public getting a third dose – Sep 23, 2021

Pfizer Inc said on Monday it has started a large study testing its investigational oral antiviral drug for the prevention of COVID-19 infection among those who have been exposed to the virus.

The drugmaker and its rivals, including U.S.-based Merck & Co Inc and Swiss pharmaceutical Roche Holding AG, have been racing to develop an easy-to-administer antiviral pill for COVID-19.

The mid-to-late-stage study will test Pfizer’s drug, PF-07321332, in up to 2,660 healthy adult participants aged 18 and older who live in the same household as an individual with a confirmed asymptomatic COVID-19 infection.

In the trial, PF-07321332, designed to block the activity of a key enzyme needed for the coronavirus to multiply, will be administered along with a low dose of ritonavir, an older medication widely used in combination treatments for HIV infection.

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To date, Gilead Sciences Inc’s intravenous drug remdesivir is the only approved antiviral treatment for COVID-19 in the United States.

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U.S. to donate half a billion additional Pfizer COVID-19 vaccines

Pfizer has also started another study of PF-07321332 in non-hospitalized, symptomatic adult patients.

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Merck and partner Ridgeback Biotherapeutics recently launched a late-stage trial of their experimental drug molnupiravir for prevention of the COVID-19 infection.

Molnupiravir is also being studied in a late-stage trial in non-hospitalized patients to see if it reduces the risk of
hospitalization or death.

(Reporting by Manojna Maddipatla and Amruta Khandekar in Bengaluru; Editing by Krishna Chandra Eluri)

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