Imperial Valley Press

FDA allows emergency use of antibody drug Trump received

- By MARILYN MARCHIONE AP Chief Medical Writer

U. S. health officials Saturday agreed to allow emergency use of a second antibody drug to help the immune system fight COVID- 19, an experiment­al medicine that President Donald Trump was given when he was sickened last month.

The Food and Drug Administra­tion authorized use of the Regeneron Pharmaceut­icals Inc. drug to try to prevent hospitaliz­ation and worsening disease from developing in patients with mild-to-moderate symptoms.

The drug is given as a one- time treatment through an IV. The FDA allowed its use in adults and children 12 and over who weigh at least 88 pounds ( 40 kilograms) and who are at high risk of severe illness from COVID-19 because of age or certain other medical conditions.

Emergency authorizat­ion allows use of the drug to start while studies are continuing to establish safety and effectiven­ess. Early results suggest the drug may reduce COVID- 19- related hospitaliz­ation or emergency room visits in patients at high risk for disease progressio­n, the FDA said.

Regeneron said that initial doses will be made available to roughly 300,000 patients through a federal government allocation program. Those patients will not be charged for the drug but may have to pay part of the cost of giving the IV.

Initial supplies will likely be vastly outstrippe­d by demand as the U. S. has surged past 12 million reported cases, with the country facing what health experts say will be a dark winter due to uncontroll­ed spread of the virus.

Antibodies are proteins the body makes to target and help eliminate viruses, but it can take weeks for the best ones to form after an infection occurs. The drugs are concentrat­ed versions of ones that proved best able to do this in lab and animal tests, and in theory help the body start to fight the virus right away.

The Regeneron drug is a combo of two antibodies to enhance the chances it will prove effective. Earlier this month, the FDA gave emergency authorizat­ion to a single-antibody drug from Eli Lilly that also is still being studied.

There’s no way to know whether the Regeneron drug helped Trump recover; he received a host of treatments and most COVID-19 patients recover on their own.

FDA regulators authorized the Regeneron drug using their emergency powers to quickly speed the availabili­ty of experiment­al drugs and other medical products during public health crises.

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