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BioWorld - Sunday, June 14, 2026
Home » Topics » Disease categories and therapies » Neurology/psychiatric

Neurology/psychiatric
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Pediatric brain illustration
Biomarkers

INDYGON syndrome, a novel spliceosomopathy caused by biallelic variants in SART3

June 22, 2023
Researchers from Murdoch Children’s Research Institute presented data from a study that linked recessive variants in the SART3 gene with a novel neurodevelopmental syndrome.
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Neurology/Psychiatric

New Cav2.3 antagonists described in Lario Therapeutics patents

June 21, 2023
Several Lario Therapeutics Ltd. patents describe new voltage-dependent R-type calcium channel subunit α-1E (Cav2.3) antagonists reported to be useful for the treatment of neurodegeneration, epilepsy, Parkinson’s disease, cerebral vasospasm, pain, CDKL5 deficiency, endocrine and neurodevelopmental disorders, among others.
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Neurology/Psychiatric

Regulus advances preclinical studies of miR-155 inhibitors for ALS

June 21, 2023
Regulus Therapeutics Inc. has provided an update on its preclinical studies evaluating a library of oligonucleotides designed to inhibit miR-155 for the treatment of amyotrophic lateral sclerosis (ALS).
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Demyelination of a neuron
Neurology/Psychiatric

Oryzon Genomics’ HDAC6 inhibitor reverses disease progression symptoms in Charcot-Marie-Tooth model

June 21, 2023
Oryzon Genomics SA has presented preclinical efficacy data on ORY-4001, a selective histone deacetylase 6 (HDAC6) inhibitor that was recently nominated as a clinical development candidate for the treatment of certain neurological diseases such as Charcot-Marie-Tooth (CMT) disease, amyotrophic lateral sclerosis and others.
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Cancer

Genentech patents new TEAD inhibitors for cancer

June 20, 2023
Transcriptional enhancer factor TEF (TEAD) inhibitors are described in a Genentech Inc. patent as potentially useful for the treatment of cancer.
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Neurology/Psychiatric

University of Sydney patent reports P2X7 receptor antagonists

June 20, 2023
The University of Sydney has patented P2X7 receptor antagonists reported to be useful for the treatment of stroke, amyotrophic lateral sclerosis, multiple sclerosis, Alzheimer’s disease, Huntington’s disease, atherosclerosis, diabetic retinopathy and myocardial infarction, among others.
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Brain-DNA illustration
Biomarkers

Variants in DMAP1 linked to new neurodevelopmental disorder

June 20, 2023
Researchers from Children’s Hospital of Philadelphia presented data from a study that linked variants in DNA methyltransferase 1-associated protein 1 (DMAP1) to a novel neurodevelopmental disorder.
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Parkinson's disease illustration showing neurons containing alpha-synuclein
Neurology/Psychiatric

Bluerock Therapeutics’ new cell therapy product shows promise for the treatment of Parkinson’s disease

June 19, 2023
Bluerock Therapeutics LP has reported the first in vitro and in vivo results on the company’s new cell therapy DA-02, consisting of human induced pluripotent stem cell (iPSC)-derived dopaminergic neurons.
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Neurology/Psychiatric

First preclinical results for VTA-100 reported by Vita Therapeutics

June 19, 2023
At the recent International Society for Stem Cell Research meeting, Vita Therapeutics Inc. presented the first preclinical results on VTA-100, a cell therapy consisting of induced pluripotent stem cell (iPSC)-derived satellite cells, for the treatment of limb-girdle muscular dystrophy 2A/R1.
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Hand holding smartphone, IA Medical chatbot icon

IA Medical raises $1.5M to develop a chatbot to support caregivers and Alzheimer's patients

June 16, 2023
By Bernard Banga
IA Medical SAS raised $1.5 million to accelerate the development of its Alix chatbot, designed to support and make life easier for caregivers of patients suffering from Alzheimer's disease. The Klesia GIE investment fund, which depends on Agirc-Arrco GIE, the administrator of the French private-sector pension scheme, and the French sovereign bank BPIFrance SA contributed 46.42% of the financing. More than half of this financing corresponds to an opening of IA Medical SAS's capital to individual partners, including doctors.
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