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Fauci: Experiment­al drug shows promise

- By Gina Kolata The New York Times

A federal trial has shown that treatment with remdesivir, an experiment­al antiviral drug, can speed recovery in patients infected with the coronaviru­s, Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, said Wednesday.

The Food and Drug Administra­tion is likely at some point to announce an emergency approval for remdesivir, a senior administra­tion official told The New York Times. Eventually the drug, made by Gilead Sciences, could be the first approved treatment for COVID-19, the illness caused by the coronaviru­s.

The virus has killed more than 60,000 people in the United States and infected more than 1 million, according to a tally by

Johns Hopkins University. Worldwide, the death toll is now at least 226,000.

Doctors and patients are desperate for an effective treatment.

Earlier Wednesday, Gilead had announced that the company was “aware of positive data” from the federal trial. Trading in the company’s stock was halted before the market opened, and the glimmer of good news drove stocks higher, despite poor economic data.

In a news briefing at the White House, Fauci and President Donald Trump hailed the early results of the federal trial, holding out hope that the drug could help very ill patients recover more quickly.

“It is a very important proof of concept, because what it has proved is that a drug can block this virus,” Fauci said.

The trial enrolled 1,063 patients who were given remdesivir or a placebo, according to the NIAID. The time to recovery averaged 11 days among those who got the drug, compared with 15 days for those who got the placebo.

There were fewer deaths in the remdesivir group, but the result did not reach statistica­l significan­ce, Fauci said. Deaths were not a primary measure in the trial.

Fauci cautioned that the results of the study still need to be properly peer reviewed, but he expressed optimism that remdesivir would become “the standard of care” for patients with COVID-19.

Dr. Robert Finberg, an investigat­or in the trial, noted that the sample was huge, and the results finished in record time.

But the disclosure of trial results in a political setting, before peer review or publicatio­n, is unusual, said Dr. Steven Nissen, a cardiologi­st at the Cleveland Clinic who has conducted dozens of clinical trials.

“Where are the data?” he asked.

Remdesivir has never been approved as a treatment for any disease. It was developed to fight Ebola, but results from a clinical trial in Africa were disappoint­ing.

The results are hard to interpret, because the study was far smaller than planned — enrolling 236 patients instead of the 453 that had been expected, because there were too few severely ill patients now in China.

Dr. Eric Peterson, a clinical trials expert at Duke University, said that with too few patients, “all you can say is it doesn’t seem to work in this population.”

If there had been a big effect of the drug, he added, that would have been seen.

 ?? MANDEL NGAN/GETTY-AFP ??
MANDEL NGAN/GETTY-AFP

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