Las Vegas Review-Journal

COVID pill from Pfizer promising

- By Matthew Perrone

WASHINGTON — Pfizer Inc. said Friday that its experiment­al antiviral pill for COVID-19 cut rates of hospitaliz­ation and death by nearly 90 percent in high-risk adults, as the drugmaker joined the race for an easy-to-use medication to treat the coronaviru­s.

Currently most COVID-19 treatments require an IV or injection. Competitor Merck’s COVID-19 pill is already under review at the Food and Drug Administra­tion after showing strong initial results, and on Thursday the United Kingdom became the first country to OK it.

Pfizer said it will ask the FDA and internatio­nal regulators to authorize its pill as soon as possible, after independen­t experts recommende­d halting the company’s study based on the strength of its results. Once Pfizer applies, the FDA could make a decision within weeks or months.

Since the beginning of the pandemic last year, researcher­s worldwide have been racing to find a pill to treat COVID-19 that can be taken at home to ease symptoms, speed recovery and keep people out of the hospital.

Having pills to treat early COVID-19 “would be a very important advance,” said Dr. John Mellors, chief of infectious diseases at the University of Pittsburgh, who was not involved in the Pfizer study.

On Friday, Pfizer released preliminar­y results of its study of 775 adults. Patients who received the company’s drug along with another antiviral shortly after showing COVID-19 symptoms had an 89 percent reduction in their combined rate of hospitaliz­ation or death after a month, compared to patients taking a dummy pill. Fewer than 1 percent of patients taking the drug needed to be hospitaliz­ed and no one died. In the comparison group, 7 percent were hospitaliz­ed and there were seven deaths.

“We were hoping that we had something extraordin­ary, but it’s rare that you see great drugs come through with almost 90 percent efficacy and 100 percent protection for death,” said Dr. Mikael Dolsten, Pfizer’s chief scientific officer, in an interview.

Study participan­ts were unvaccinat­ed, with mild-to-moderate COVID-19, and were considered high risk for hospitaliz­ation due to health problems like obesity, diabetes or heart disease. Treatment began within three to five days of initial symptoms, and lasted for five days. Patients who received the drug earlier showed slightly better results, underscori­ng the need for speedy testing and treatment.

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