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BioWorld - Thursday, June 18, 2026
Home » Topics » Disease categories and therapies » Neurology/psychiatric

Neurology/psychiatric
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CSPG signaling modulator NVG-291 improves experimental stroke recovery

Aug. 5, 2022
After stroke, chondroitin sulfate proteoglycans (CSPGs) inhibit neuroblast migration and axon sprouting, but these effects can be blunted by modulating receptor-type tyrosine-protein phosphatase S (PTPsigma).
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Chronic oral treatment with ERbeta agonist EGX-358 evaluated in Alzheimer's disease mouse model

Aug. 4, 2022
Data from preclinical studies conducted to examine the activities of the novel estrogen receptor beta (ERbeta) agonist EGX-358, previously under study for the treatment of hot flushes at Estrigenix Therapeutics, for the potential treatment of Alzheimer's disease (AD) were presented at the recent Alzheimer's Association International Conference.
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Dong-A ST compound DA-7503 potently inhibits tau aggregation

Aug. 3, 2022
At the Alzheimer's Association International Conference, Dong-A ST scientists described preclinical research on a new tau-targeted agent, DA-7503.
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Design Therapeutics divulges new frataxin modulators

Aug. 3, 2022
Design Therapeutics has discovered conjugates consisting of a DNA-binding moiety capable of noncovalently binding to a nucleotide repeat sequence linked to a protein-binding moiety through an oligomeric backbone linker reported to be useful for the treatment of Friedreich ataxia.
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ADHD carved into desktop

Shionogi begins pivotal trial of Akili’s ADHD digital therapy in Japan

Aug. 2, 2022
By Meg Bryant
Akili Interactive Labs Inc. has kicked off a phase III study of its digital treatment for children with attention-deficit/hyperactivity disorder (ADHD) living in Japan, the first pivotal trial of its video game-based cognitive treatment outside the U.S. Conducted by Osaka-based Shionogi & Co. Ltd., this marks the first pivotal trial of Akili’s video game-based cognitive treatment outside the U.S.
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Elderly hands holding broken brain structure

Cognetivity works to expand awareness, potential uses of brain health test

Aug. 2, 2022
By Nuala Moran
Cognetivity Neurosciences Ltd. is making progress in promoting its cognitive assessment tool as the brain health equivalent of a blood pressure check, following feedback from clinicians indicating the test could have broad applicability.
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Handshake dollar sign

Back for more: Sosei and Abbvie cut another $1B+ deal

Aug. 2, 2022
By Lee Landenberger
Sosei Heptares and Abbvie Inc. have built on the huge, multitarget deal they cut a little more than two years ago by signing another one.
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Amyloid plaques forming between neurons

AAIC 2022: The BACE1 inhibition comeback

Aug. 2, 2022
By Brian Orelli
Beta-site APP-cleaving enzyme 1 (BACE1) inhibitors have a long history of failure in patients with Alzheimer’s disease. Clinical development of verubecestat, elenbecestat, lanabecestat, umibecestat, atabecestat and LY-3202626 were all discontinued. The drugs largely showed that inhibiting BACE1 reduced amyloid beta (AB) in both cerebrospinal fluid and plasma, reduced AB plaques on PET scans and reduced phosphorylated tau. Unfortunately, patients had early cognitive worsening, and there were signs of lowering of brain volume and increases in psychiatric adverse events.
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Sosei Heptares and AbbVie announce new multi-target drug discovery collaboration

Aug. 2, 2022
Sosei Group Corporation and AbbVie have entered a new drug discovery collaboration and option-to-license agreement to discover, develop and commercialize small molecules that modulate novel G protein-coupled receptor (GPCR) targets associated with neurological disease.
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AAIC 2022

Lessons learned from a decade following familial frontotemporal dementia patients

Aug. 1, 2022
By Brian Orelli
During a presentation at the Alzheimer's Association International Conference 2022, researchers from the Genetic Frontotemporal Dementia (FTD) Initiative consortium presented data from a study following nearly 1,300 patients with FTD caused by a genetic mutation, their presymptomatic family members who have the inherited mutation and unaffected family members to serve as controls. Researchers have used data from the study, which has been enrolling patients for over 10 years, to develop biomarkers that can be used to assess progression of FTD in interventional clinical trials.
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