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		<title>FDA Approves Blood Test Developed by Abbott, USAMMDA for Traumatic Brain Injury</title>
		<link>https://innovate.research.ufl.edu/tba-blood-test/</link>
		
		<dc:creator><![CDATA[Sara Dagen]]></dc:creator>
		<pubDate>Mon, 06 May 2024 00:00:00 +0000</pubDate>
				<category><![CDATA[News Brief]]></category>
		<category><![CDATA[UF Inventors]]></category>
		<category><![CDATA[UF Startup]]></category>
		<category><![CDATA[Abbott Laboratories]]></category>
		<category><![CDATA[Abbott Point of Care]]></category>
		<category><![CDATA[Banyan Biomarkers]]></category>
		<category><![CDATA[biomarkers]]></category>
		<category><![CDATA[blood test]]></category>
		<category><![CDATA[i-STAT Alinity]]></category>
		<category><![CDATA[Kevin Wang]]></category>
		<category><![CDATA[Ron Hayes]]></category>
		<category><![CDATA[traumatic brain injury]]></category>
		<category><![CDATA[U.S. Army]]></category>
		<category><![CDATA[USAMMDA]]></category>
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					<description><![CDATA[The U.S. Food and Drug Administration recently approved a blood test the U.S. Army Medical Materiel Development Activity at Fort Detrick worked on with Abbott Point of Care, which can detect signs of traumatic brain injury more quickly than a previous test by UF startup Banyan Biomarkers. Banyan's biomarkers are used in the new device.]]></description>
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<p>The U.S. Food and Drug Administration recently approved a blood test the U.S. Army Medical Materiel Development Activity at Fort Detrick worked on with Abbott Point of Care, which can detect signs of traumatic brain injury more quickly than a previous test by UF startup Banyan Biomarkers. Banyan&#8217;s biomarkers are used in the new device.</p>



<p>The i-STAT Alinity, a device created by Abbott, can test blood samples on a specific cartridge that USAMMDA developed and can deliver results in about 15 minutes. The device detects if a blood sample has elevated levels of specific biological markers, which indicate a brain bleed or injury.</p>



<p>If the sample has those elevated biological markers, the person can be transported from areas of combat to a hospital for a CT scan, USAMMDA product manager Damien Hoffman said.</p>



<p>USAMMDA develops new vaccines, drugs, devices, and other medical support equipment and leads medical product development for the U.S. Army. Abbott Point of Care is a division of Abbott Laboratories, a medical devices and healthcare company.</p>



<p>In 2018, UF startup Banyan Biomarkers received FDA approval for a blood test that detects the presence of two specific biomarkers — UCH-L1 and GFAP — to determine if a person has a mild brain injury. Banyan&#8217;s technology, which provides results in 3-4 hours, was discovered by a team of UF researchers, including Drs. Kevin Wang (Department of Psychiatry) and Ron Hayes (Department of Neuroscience) in the College of Medicine. </p>



<p>In 2019, Abbott received licensure from Banyan to use the company’s biomarkers on Abbott’s i-STAT Alinity device.</p>



Read more about <a href="https://www.fredericknewspost.com/news/health/fda-approves-blood-test-developed-by-abbott-usammda-for-traumatic-brain-injury/article_6a720b13-be94-586a-99a1-65097f6f62ff.html">FDA Approves Blood Test Developed by Abbott, USAMMDA for Traumatic Brain Injury.</a>
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