{"id":38700,"date":"2020-03-23T11:21:34","date_gmt":"2020-03-23T15:21:34","guid":{"rendered":"https:\/\/sciencebusiness.technewslit.com\/?p=38700"},"modified":"2020-03-23T11:21:34","modified_gmt":"2020-03-23T15:21:34","slug":"fda-okays-faster-covid-19-test-nixes-home-tests","status":"publish","type":"post","link":"https:\/\/technewslit.com\/sciencebusiness\/?p=38700","title":{"rendered":"FDA Okays Faster Covid-19 Test, Nixes Home Tests"},"content":{"rendered":"<figure id=\"attachment_38608\" aria-describedby=\"caption-attachment-38608\" style=\"width: 640px\" class=\"wp-caption aligncenter\"><a href=\"https:\/\/technewslit.com\/sciencebusiness\/wp-content\/uploads\/2020\/03\/Coronavirus_PeteLinforth_Pixabay.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"size-full wp-image-38608\" src=\"https:\/\/technewslit.com\/sciencebusiness\/wp-content\/uploads\/2020\/03\/Coronavirus_PeteLinforth_Pixabay.jpg\" alt=\"Coronavirus graphic\" width=\"640\" height=\"320\" srcset=\"https:\/\/technewslit.com\/sciencebusiness\/wp-content\/uploads\/2020\/03\/Coronavirus_PeteLinforth_Pixabay.jpg 640w, https:\/\/technewslit.com\/sciencebusiness\/wp-content\/uploads\/2020\/03\/Coronavirus_PeteLinforth_Pixabay-300x150.jpg 300w, https:\/\/technewslit.com\/sciencebusiness\/wp-content\/uploads\/2020\/03\/Coronavirus_PeteLinforth_Pixabay-150x75.jpg 150w, https:\/\/technewslit.com\/sciencebusiness\/wp-content\/uploads\/2020\/03\/Coronavirus_PeteLinforth_Pixabay-400x200.jpg 400w\" sizes=\"auto, (max-width: 640px) 100vw, 640px\" \/><\/a><figcaption id=\"caption-attachment-38608\" class=\"wp-caption-text\">(Pete Linforth, Pixabay)<\/figcaption><\/figure>\n<p>23 Mar. 2020. The Food and Drug Administration granted an emergency clearance for a point-of-care test to detect for the virus causing novel coronavirus or Covid-19 infections. The agency also put a hold for now on authorizations for home testing or sample collection kits.<\/p>\n<p>FDA on Saturday <a href=\"https:\/\/www.fda.gov\/news-events\/press-announcements\/coronavirus-covid-19-update-fda-issues-first-emergency-use-authorization-point-care-diagnostic\">cleared<\/a> the Xpert Xpress Sars-CoV-2 test made by <a href=\"https:\/\/www.cepheid.com\/\">Cepheid<\/a>, a molecular diagnostics company in Sunnyvale, California. The <a href=\"https:\/\/www.cepheid.com\/coronavirus\">Xpert Xpress Sars-CoV-2<\/a> test reads a person&#8217;s nose swab specimen taken by a clinician. The specimen is then mixed with reagents in a cartridge that fits into Cepheid&#8217;s <a href=\"https:\/\/www.cepheid.com\/en_US\/systems\/GeneXpert-Family-of-Systems\/GeneXpert-Xpress\">GeneXpert<\/a> analysis system. The GeneXpert system conducts a reverse transcription-polymerase chain reaction, or <a href=\"https:\/\/www.thermofisher.com\/us\/en\/home\/references\/ambion-tech-support\/rtpcr-analysis\/general-articles\/rt--pcr-the-basics.html\">RT-PCR analysis<\/a> that identifies and quantifies messenger RNA in the sample, in this case RNA signatures indicating the presence of Sars-CoV-2 viruses responsible for Covid-19 infections.<\/p>\n<p>Cepheid says its system can return results in 45 minutes, once the GeneXpert system runs the test. &#8220;Cepheid currently has nearly 5,000 GeneXpert systems in the U.S. capable of point-of-care testing and for use in hospitals,&#8221; says company president <a href=\"https:\/\/www.linkedin.com\/in\/warren-kocmond-1b8160a\/\">Warren Kocmond<\/a> in a <a href=\"http:\/\/cepheid.mediaroom.com\/2020-03-21-Cepheid-Receives-Emergency-Use-Authorization-from-FDA-for-Rapid-SARS-CoV-2-Test\">company statement<\/a>. &#8220;Our automated systems do not require users to have specialty training to perform testing. They are capable of running 24\/7, with many systems already doing so today.&#8221;<\/p>\n<p>FDA cleared the Xpert Xpress Sars-CoV-2 test under an <a href=\"https:\/\/www.fda.gov\/emergency-preparedness-and-response\/mcm-legal-regulatory-and-policy-framework\/emergency-use-authorization\">emergency use authorization<\/a>, an exemption from normal review procedures employed by the agency during public heath emergencies. The <a href=\"https:\/\/www.fda.gov\/media\/136316\/download\">authorization<\/a> clears the test when analyzed in labs certified for high and moderate complexity testing under the <a href=\"https:\/\/www.fda.gov\/medical-devices\/ivd-regulatory-assistance\/clinical-laboratory-improvement-amendments-clia\">Clinical Laboratory Improvement Amendments<\/a> process, and specifically allows for use in patient-care settings. Most other Covid-19 virus tests require shipping the samples to separate labs for analysis.<\/p>\n<p>The lack of rapid and widespread Covid-19 testing is <a href=\"https:\/\/www.sciencemag.org\/news\/2020\/03\/i-m-going-keep-pushing-anthony-fauci-tries-make-white-house-listen-facts-pandemic\">hampering the U.S. response<\/a> to the pandemic. As of this morning (23 Mar.) the U.S. and its territories conducted 236,006 patient tests, with 32,617 testing positive and 203,389 negative, according to the <a href=\"https:\/\/covidtracking.com\/data\/\">Covid Tracking Project<\/a>, a volunteer web site. The worldwide <a href=\"https:\/\/www.arcgis.com\/apps\/opsdashboard\/index.html#\/bda7594740fd40299423467b48e9ecf6\">Covid-19 tracking dashboard<\/a> hosted by Johns Hopkins University shows 35,225 cases in the U.S., about 10 percent of the worldwide total, responsible for 473 deaths.<\/p>\n<p>FDA, however, is not authorizing tests for Covid-19 viruses at home, at least for now. On Thursday, 20 Mar., the agency issued a warning about <a href=\"https:\/\/www.fda.gov\/news-events\/press-announcements\/coronavirus-covid-19-update-fda-alerts-consumers-about-unauthorized-fraudulent-covid-19-test-kits\">fraudulent home testing kits<\/a> being marketed in the U.S. &#8220;We want to alert the American public,&#8221; says the FDA statement, &#8220;that at this time, the FDA has not authorized any test that is available to purchase for testing yourself at home for COVID-19.&#8221;<\/p>\n<p>An agency FAQs page on <a href=\"https:\/\/www.fda.gov\/medical-devices\/emergency-situations-medical-devices\/faqs-diagnostic-testing-sars-cov-2\">diagnostic testing<\/a> posted over the weekend also notes, &#8220;At this time, the FDA has not authorized any test that is available to purchase for testing yourself at home for COVID-19. The FDA sees the public health value in expanding the availability of COVID-19 testing through safe and accurate tests that may include home collection, and we are actively working with test developers in this space.&#8221;<\/p>\n<p>FDA&#8217;s policy puts on hold for now plans by a few home test kit developers for other conditions to immediately offer home sample collection or point-of-care tests for the Covid-19 virus. The technology news service <a href=\"https:\/\/techcrunch.com\/2020\/03\/23\/updated-fda-covid-19-testing-guidelines-specifically-disallows-at-home-sample-colllection\/\">TechCrunch<\/a> reports that one company already collecting nasal swab samples from customers is destroying those samples.<\/p>\n<p>More from Science &amp; Enterprise:<\/p>\n<ul>\n<li><a href=\"https:\/\/sciencebusiness.technewslit.com\/?p=38695\">Infographic \u2013 National Coronavirus Case Severity<\/a><\/li>\n<li><a href=\"https:\/\/sciencebusiness.technewslit.com\/?p=38690\">Univ Labs Developing Covid-19, Outbreak Test Devices<\/a><\/li>\n<li><a href=\"https:\/\/sciencebusiness.technewslit.com\/?p=38676\">WHO Beginning Covid-19 Therapy Trial<\/a><\/li>\n<li><a href=\"https:\/\/sciencebusiness.technewslit.com\/?p=38669\">FDA Outlines Trial Disruption Steps Due to Covid-19<\/a><\/li>\n<li><a href=\"https:\/\/sciencebusiness.technewslit.com\/?p=38658\">Case Study Maps Covid-19 Immune Response<\/a><\/li>\n<\/ul>\n<p style=\"text-align: center;\">*\u00a0\u00a0\u00a0\u00a0 *\u00a0\u00a0\u00a0\u00a0 *<\/p>\n","protected":false},"excerpt":{"rendered":"<p>The Food and Drug Administration granted an emergency clearance for a point-of-care test to detect for the virus causing novel coronavirus or Covid-19 infections.<\/p>\n","protected":false},"author":1,"featured_media":38608,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[5],"tags":[31,140,86,22,55,95,64,77],"class_list":["post-38700","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-regulations","tag-biomedical","tag-covid19","tag-engineering","tag-fda","tag-genomics","tag-health-care","tag-life-sciences","tag-medical-device"],"_links":{"self":[{"href":"https:\/\/technewslit.com\/sciencebusiness\/index.php?rest_route=\/wp\/v2\/posts\/38700","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/technewslit.com\/sciencebusiness\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/technewslit.com\/sciencebusiness\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/technewslit.com\/sciencebusiness\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/technewslit.com\/sciencebusiness\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=38700"}],"version-history":[{"count":2,"href":"https:\/\/technewslit.com\/sciencebusiness\/index.php?rest_route=\/wp\/v2\/posts\/38700\/revisions"}],"predecessor-version":[{"id":38702,"href":"https:\/\/technewslit.com\/sciencebusiness\/index.php?rest_route=\/wp\/v2\/posts\/38700\/revisions\/38702"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/technewslit.com\/sciencebusiness\/index.php?rest_route=\/wp\/v2\/media\/38608"}],"wp:attachment":[{"href":"https:\/\/technewslit.com\/sciencebusiness\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=38700"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/technewslit.com\/sciencebusiness\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=38700"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/technewslit.com\/sciencebusiness\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=38700"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}