Over-the-counter home test for COVID-19 gets US green light

Tuesday, December 15, 2020

WASHINGTON (AP) — The first home test for COVID-19 that doesn’t require a prescription will soon be on U.S. store shelves.

U.S. regulators Tuesday authorized the rapid coronavirus test, which can be done entirely at home. The announcement by the Food and Drug Administration represents another important — though incremental — step in efforts to expand testing options.

The agency’s action allows the test to be sold in places like drugstores “where a patient can buy it, swab their nose, run the test and find out their results in as little as 20 minutes,” said FDA Commissioner Stephen Hahn, in a statement. Regulators granted emergency use for a similar home test last month, but that one requires a doctor’s prescription. Initial supplies of the over-the-counter test will be limited. Australian manufacturer Ellume said it expects to produce 3 million tests next month before ramping up production over the first half of 2021.

A company spokesperson said the test will be priced around $30 and be available at pharmacies and for purchase online.

The kit includes a nasal swab, a chemical solution and a testing strip. The test connects digitally to a smart phone app that displays the results and then helps interpret the results. Users can also connect with a health professional via the app.

Like other tests that scan for proteins, FDA officials noted that Ellume’s test can deliver a small percentage of false positive and false negative results. People who get a negative result but have coronavirus symptoms should follow up with a health professional, the agency said.

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