… Florida’s medical marijuana dispensaries. “At all times, I acted lawfully and in full alignment with SOS’s mission,” wrote Ronshausen, who seeks …
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Tennessee’s Governor Must Veto Hemp Restriction Bill That Would Take CBD Products …
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Nebraska Governor Announces Support For Medical Cannabis Commission As Lawmakers …
“The Medical Cannabis Commission is fully enabled to meet and carry out its responsibilities.” By Zach Wendling, Nebraska Examiner.
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Pennsylvania GOP Senator Pushes To Create New Marijuana Regulatory Body While …
… marijuana, calling it “the most conservative stance” on the issue. DeSantis Signs Bill To Criminalize Psychedelic Mushroom Spores In Florida …
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Winning numbers drawn in Friday’s Florida Pick 5 Evening – New Haven Register
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420 with CNW — Florida Advocacy Group Joins Legal Challenge to State’s Initiatives Law
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FDA OKs first blood test that can help diagnose Alzheimer’s disease
By MATTHEW PERRONE
WASHINGTON (AP) — U.S. health officials on Friday endorsed the first blood test that can help diagnose Alzheimer’s and identify patients who may benefit from drugs that can modestly slow the memory-destroying disease.
The test can aid doctors in determining whether a patient’s memory problems are due to Alzheimer’s or a number of other medical conditions that can cause cognitive difficulties. The Food and Drug Administration cleared it for patients 55 and older who are showing early signs of the disease.
More than 6 million people in the United States and millions more around the world have Alzheimer’s, the most common form of dementia.
The new test, from Fujirebio Diagnostics, Inc., identifies a sticky brain plaque, known as beta-amyloid, that is a key marker for Alzheimer’s. Previously, the only FDA-approved methods for detecting amyloid were invasive tests of spinal fluid or expensive PET scans.
The lower costs and convenience of a blood test could also help expand use of two new drugs, Leqembi and Kisunla, which have been shown to slightly slow the progression of Alzheimer’s by clearing amyloid from the brain. Doctors are required to test patients for the plaque before prescribing the drugs, which require regular IV infusions.
“Today’s clearance is an important step for Alzheimer’s disease diagnosis, making it easier and potentially more accessible for U.S. patients earlier in the disease,” said Dr. Michelle Tarver, of FDA’s center for devices.
A number of specialty hospitals and laboratories have already developed their own in-house tests for amyloid in recent years. But those tests aren’t reviewed by the FDA and generally aren’t covered by insurance. Doctors have also had little data to judge which tests are reliable and accurate, leading to an unregulated marketplace that some have called a “wild west.”
Several larger diagnostic and drug companies are also developing their own tests for FDA approval, including Roche, Eli Lilly and C2N Diagnostics.
The tests can only be ordered by a doctor and aren’t intended for people who don’t yet have any symptoms.
AP Medical Writer Lauran Neergaard contributed to this story
The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute’s Science and Educational Media Group. The AP is solely responsible for all content.
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Members Of Congress Want Federal Investigation Into Use Of Florida Medicaid Funds To …
The money was used to fight against a citizen ballot initiative, vehemently opposed by DeSantis, that would have legalized marijuana for adults. Reps.
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Woman caught at airport with over 40 pounds of marijuana in her suitcases, authorities say
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