February 14th, 2018
The FDA has approved the first blood test to help diagnose
concussions, clearing a path to the market for a diagnostic that could reduce
the use of expensive brain imaging technologies that expose patients to
radiation.
The approval goes to San Diego diagnostics
developer Banyan Biomarkers. The company’s test, called Banyan BTI (short for
brain trauma indicator), measures the levels of two proteins that the brain
releases into the blood in the hours following a head injury. The company
developed the test with partial support from a contract with the U.S. Army.
The current standard for concussion diagnosis
involves a neurological assessment that measures a patient’s eye, verbal, and
motor responses. That assessment is followed by a computed tomography (CT)
scan. Banyan says that measuring the levels of the two
brain proteins can help clinicians determine whether or not to proceed with a
CT scan. The company’s test returns results within four hours.
Banyan’s test was evaluated in a study that
enrolled more than 2,000 adult patients in the U.S. and Europe suspected to
have a concussion. Blood test results were compared to CT scans. The FDA says
the Banyan test was able to predict the presence of brain injury on a CT scan
97.5 percent of the time. For those who did not have a brain injury, the Banyan
test was correct 99.6 percent of the time. Using the test could rule out the
need for CT scans in at least one-third of suspected concussion patients, the
FDA says.
Banyan is conducting more studies to determine
if its tests could be used to monitor a patient’s recovery from injury. The company
is also studying how its tests could be used to assess other brain conditions.
The FDA reviewed the Banyan test under its
“Breakthrough Devices Program,” which was added under the 21st Century Cures Act, a wide-ranging 2016 law that includes
provisions for speeding up the review of medical devices and drugs to
bring new products to the market faster.
Because Banyan BTI is the first blood test for
brain injury that the FDA has approved for sale, its approval creates a new
classification for these types of diagnostics. That means going forward, the
Banyan test will be the basis upon which the FDA reviews new blood tests for
brain injury developed by Banyan or other companies.
https://www.xconomy.com/san-diego/2018/02/14/fda-o-k-s-banyan-diagnostic-the-first-blood-test-for-concussions/?itx[idio]=8812325&ito=792&itq=d788768b-5f34-4b97-b93d-d084d57dbe65
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