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

Neurology/psychiatric
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Wellstat Therapeutics divulges novel uridine derivatives

June 29, 2022
Stroke illustration: brain, artery, neurons

Duo of Peijia catheters approved in China for neurointerventional surgery

June 28, 2022
By Doris Yu
Peijia Medical Ltd. has received two marketing approvals from China’s NMPA for its catheters to be used in neurointerventional surgery. They are the balloon guide catheter (BGC) Fluxcap and delivery balloon dilation catheter Fastunnel. Both were developed by Peijia’s wholly owned subsidiary Achieva Medical Ltd.
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Conference data for June 28, 2022: EAN

June 28, 2022
New and updated preclinical and clinical data presented by biopharma firms at the European Academy of Neurology Congress, including: Bristol Myers Squibb, Horizon, Teva.
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Tract mapping in the human brain
EAN 2022

At several scales, connective landscape provides lens for neurology

June 28, 2022
By Anette Breindl
Connections, Susan Greenfield told her audience at the 2022 Annual Conference of the European Academy of Neurology, are what the mind is all about. "When you are born, you are born with a fair amount of neurons," she said at the conference's opening plenary on Sunday. But "what characterizes the growth of the brain postnatally is the configurations of connections."
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EAN 2022: At several scales, connective landscape provides lens for neurology

June 28, 2022

MagicMed Industries discloses new 5-HT2A receptor agonists

June 28, 2022
FDA icons

Axsome receives proposed US FDA labeling for AXS-05

June 27, 2022
By Lee Landenberger
Axsome Therapeutics Inc. and the U.S. FDA appear to be working out their differences. The company said it received the proposed labeling from the agency for AXS-05 (dextromethorphan + bupropion), an oral NMDA receptor antagonist with multimodal activity, for treating major depressive disorder.
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SAGE Therapeutics describes new GABA-A receptor modulators

June 27, 2022

Uniqure reassures with full-year low-dose data in HD; efficacy ahead with gene therapy?

June 23, 2022
By Randy Osborne
Uniqure NV rolled out stock-pleasing safety and biomarker data from 10 patients enrolled in the low-dose cohort of the ongoing phase I/II trial with AMT-130 for the treatment of Huntington’s disease (HD), but investors must wait for details on MRI scans. “We have communicated that we will discuss the MRI findings in the middle of next year,” CEO Matt Kapusta told investors during a conference call. “That’s all I can say.”
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Mindset Pharma collaborates with CAMH on preclinical evaluation of MSP-1014

June 23, 2022
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