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BioWorld - Wednesday, December 24, 2025
Home » Alzheimer’s disease

Articles Tagged with ''Alzheimer’s disease''

How it works diagram: Step 1 task image displayed, Step 2 eye tracking, Step 3 cognitive scoring

Otsuka to market Ai-Brainscience’s eye-tracking cognitive test app in Japan

May 24, 2022
By Tamra Sami
Otsuka Pharmaceutical Co. Ltd. and Ai-Brainscience Inc. signed an exclusive sales agreement for Japan that will see Otsuka market Ai-Brainscience’s eye-tracking application to test for cognitive function. The eye-tracking app, AiBS-01, could become the first dementia diagnosis application to receive regulatory approval in Japan. Ibaraki, Japan-based Ai-Brainscience (AiBS) is developing devices that use the eye-tracking based cognitive assessment test to detect early dementia beyond the conventional assessment methods performed by specialists.
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Lumipulse-G

FDA grants Fujirebio first marketing authorization for in vitro diagnostic for Alzheimer’s

May 5, 2022
By Annette Boyle
Mark it as a day to remember. The U.S. FDA has awarded de novo marketing authorization for the first in vitro diagnostic (IVD) test for Alzheimer’s disease (AD), enabling diagnosis of the dreaded disease years earlier than current clinical tests. Fujirebio Diagnostics Inc.’s Lumipulse G β-Amyloid Ratio (1-42/1-40) measures specific proteins in cerebral spinal fluid to provide rapid assessment of the risk of amyloid plaques, an indicator of the disease that may develop decades before cognitive impairment occurs.
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FDA grants Fujirebio first marketing authorization for in vitro diagnostic for Alzheimer’s

May 5, 2022
By Annette Boyle
Mark it as a day to remember. Today the FDA authorized the first in vitro diagnostic test for Alzheimer’s disease, enabling diagnosis of the dreaded disease years earlier than current clinical tests. Fujirebio Diagnostics Inc.’s Lumipulse G β-Amyloid Ratio (1-42/1-40) measures specific proteins in cerebral spinal fluid to provide rapid assessment of the risk of amyloid plaques, an indicator of the disease that may develop decades before cognitive impairment occurs.
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Biogen logo

Aduhelm claims Biogen’s CEO as a victim as the failure ripples outward

May 3, 2022
By Lee Landenberger
The flop that is Aduhelm (aducanumab) made itself felt in Biogen Inc.’s executive suite as CEO Michael Vounatsos is leaving the company. He had the job for five and a half years and for less than a year after the controversial Alzheimer’s treatment was approved. He will stick around until a successor is found.
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Medicare puzzle

US CMS told to stay in its lane on coverage decisions

May 3, 2022
By Mari Serebrov
The U.S. Centers for Medicare & Medicaid Services’ (CMS) decision last month restricting coverage of a class of Alzheimer’s drugs to clinical trials meeting the agency’s standards still isn’t sitting well with some lawmakers.
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Becerra on the hot seat in US House budget hearing

April 27, 2022
By Mari Serebrov
Making his first in-person appearance April 27 before the House Energy and Commerce Subcommittee on Health, U.S. Health and Human Services Secretary Xavier Becerra was prepared to answer questions about President Joe Biden’s fiscal 2023 budget that would increase HHS’ discretionary budget to $127 billion, nearly a 27% increase over the 2021 enacted level.
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Walking with assistance
Newco news

Mitorx tackling impaired sulphide signaling in degenerative disease

April 26, 2022
By Nuala Moran
Mitorx Therapeutics Ltd. is poised to develop small molecules that reverse impaired sulphide signaling underlying degenerative diseases ranging from Duchenne muscular dystrophy to Alzheimer’s disease. The company was formed some time ago as a spinout from Exeter University, where the founding scientist Matt Whiteman is professor of experimental therapeutics. It is showing its colors for the first time after closing a seed funding round.
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Aduhelm product image

Biogen withdraws EU Aduhelm filing amid announcement of latest CHMP opinions

April 22, 2022
By Richard Staines
Biogen Inc. has given up on its attempt to get its Alzheimer’s disease drug Aduhelm (aducanumab) approved by regulators in Europe, deciding to withdraw its filing midway through a review of a previous rejection. The company had asked the European Medicines Agency’s CHMP to reconsider its negative opinion for Aduhelm in December 2021. But its subsidiary in the Netherlands wrote to the EMA this week saying that it had decided to withdraw its marketing authorization application after all.
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Elderly hands holding broken brain structure

‘Aduhelm’ of ship in AD drug access, CMS wrongly captain of patient choice?

April 8, 2022
By Randy Osborne
The release by the U.S. CMS of the final national coverage determination (NCD) for Biogen Inc.’s Alzheimer disease (AD) drug, Aduhelm (aducanumab), lit speculation on the meaning for others in the space. CMS is “still being conservative,” said Howard Fillit, co-founder and chief science officer of the Alzheimer’s Drug Discovery Foundation (ADDF). “We’re in a new era. It’s unprecedented that Medicare doesn’t pay for a drug that received approval from the FDA,” even though it was not a full but an accelerated clearance.
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Elderly hands holding broken brain structure

Alternate approach could enable earlier detection, intervention, in Alzheimer's

April 7, 2022
By Nuala Moran
Neuro-Bio Ltd. has published animal data it says confirms its hypothesis about an underlying cause of Alzheimer's and showing its lead molecule NBP-14 decreases levels of brain amyloid and restores memory in a mouse model of the disease.
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