Selective serotonin reuptake inhibitor

Hedonia’s Chief Scientific Officer, Professor Moshe Bar, explains: What is Facilitating Thought Progression (FTP)?

Retrieved on: 
Monday, July 10, 2023

That’s the basis for facilitating thought progression, FTP for short.

Key Points: 
  • That’s the basis for facilitating thought progression, FTP for short.
  • FTP is a new adjunct therapy delivered through mobile games that patients play for 15 to 30 minutes daily.
  • FTP is designed to disrupt tormenting thinking patterns, lack of motivation, and the inability to experience pleasure, which are characteristic of mood disorders.
  • In other words, facilitating thought progression could improve individuals’ moods through noninvasive, simple exercises that would encourage them to:
    Broaden their thought patterns to be more associative.

Small Pharma Reports Financial Results for the Fiscal Year Ended February 28, 2023 and Recent Business Highlights

Retrieved on: 
Wednesday, June 28, 2023

LONDON, June 28, 2023 (GLOBE NEWSWIRE) -- Small Pharma Inc. (TSXV: DMT) (OTCQB: DMTTF) (the “Company” or “Small Pharma”), a biotechnology company focused on short-duration psychedelic-assisted therapies for mental health conditions, has today published its financial results for the fiscal year ended February 28, 2023. A complete copy of the audited consolidated financial statements prepared in accordance with International Financial Reporting Standards and the corresponding management’s discussion and analysis can be found under the Company’s profile on SEDAR at www.sedar.com. Unless otherwise indicated, all currency references are in Canadian dollars.

Key Points: 
  • LONDON, June 28, 2023 (GLOBE NEWSWIRE) -- Small Pharma Inc. (TSXV: DMT) (OTCQB: DMTTF) (the “Company” or “Small Pharma”), a biotechnology company focused on short-duration psychedelic-assisted therapies for mental health conditions, has today published its financial results for the fiscal year ended February 28, 2023.
  • Financial Highlights (including post-period events)1:
    Cash on hand as of February 28, 2023 was approximately $18.5 million.
  • Cash used in operating activities was $22.2 million for the 12 months ended February 28, 2023.
  • Small Pharma has advanced its clinical program of SPL026, with ongoing exploratory studies to evaluate additional formulations and treatment populations.

People with obsessive-compulsive disorder have an imbalance of brain chemicals – our discovery could mean a treatment breakthrough

Retrieved on: 
Wednesday, June 28, 2023

But OCD is actually a severe and disabling disorder characterised by obsessions – recurrent intrusive thoughts, impulses or images that are unwanted and anxiety provoking.

Key Points: 
  • But OCD is actually a severe and disabling disorder characterised by obsessions – recurrent intrusive thoughts, impulses or images that are unwanted and anxiety provoking.
  • Some people with OCD are engaged in rituals for much of their waking life and cannot even leave their homes.
  • But in our new research, published in Nature Communications, we discovered an imbalance in brain chemicals in OCD that could lead to radically different and improved treatments.
  • Scientists have suspected that this involves an imbalance between chemical messengers, or neurotransmitters, called
    glutamate and gamma-aminobutyric acid (Gaba) in certain brain regions.

Magnetic resonance spectroscopy

    • To study glutamate and Gaba, we used a high-strength magnet (called 7-Tesla) to perform magnetic resonance spectroscopy.
    • This helps scientists to measure what kind of chemicals exist there – and their concentration.
    • This allowed us to detect and measure glutamate and Gaba levels separately in different brain regions.
    • Importantly, the clinical severity of compulsive symptoms of OCD correlated with the glutamate levels we measured in the SMA.

Future treatments

    • The finding raises hopes for better treatments for OCD, focusing on re-balancing glutamate and Gaba levels in key brain regions.
    • In patients with extremely severe OCD, for whom all other usual treatments have failed, surgeons have actually removed the ACC.
    • And for less severely impaired patients where such drastic treatments are not justified, there may be therapeutic possibilities of using “transcranial magnetic stimulation”.
    • In future, if OCD is diagnosed early in the course of the illness – and the chemical imbalance we have discovered is also detected – then these new treatments offer hope for improved quality of life and wellbeing for patients the disorder.

Cognigenics' Intranasal CRISPR Delivery Bypasses Blood-Brain Barrier; Potential Breakthrough Therapeutic

Retrieved on: 
Thursday, June 22, 2023

Cognigenics CEO John L. Mee announces breakthrough results from an animal study published today in PNAS Nexus.

Key Points: 
  • Cognigenics CEO John L. Mee announces breakthrough results from an animal study published today in PNAS Nexus.
  • The findings point to the potential of non-invasively delivering neuromodulating gene therapies to the brain for chronic mental health conditions using adeno-associated viruses introduced intranasally.
  • The method requires two delivery vectors because of the limited cargo capacity of the viruses.
  • Each virus was modified using Cognigenics' proprietary CRISPR gene-editing technology.

Tonix Pharmaceuticals Announces Pharmacology and Medicinal Chemistry Results that Reveal the Molecular Mechanism of Action of Tianeptine, the Active Ingredient of TNX-601 ER, in Treating Depression

Retrieved on: 
Wednesday, May 17, 2023

CHATHAM, N.J., May 17, 2023 (GLOBE NEWSWIRE) -- Tonix Pharmaceuticals Holding Corp. (Nasdaq: TNXP) (Tonix or the Company), a clinical-stage biopharmaceutical company, today announced the molecular mechanism of action of tianeptine, the active ingredient of TNX-601 ER (tianeptine hemioxalate extended-release tablets), currently in Phase 2 clinical development for the treatment of major depressive disorder (MDD)*. Based on pharmacology and medicinal chemistry experiments, scientists at Tonix have established that tianeptine is an agonist for the nuclear peroxisome proliferator-activated receptor (PPAR) isoforms PPAR-β/δ and PPAR-γ, and tianeptine’s effects on these PPAR isoforms account for its ability to induce neuroplasticity in cultured neurons.

Key Points: 
  • Drugs that restore neuroplasticity are called plastogens.1-3 Consequently, tianeptine is a plastogen that acts directly on nuclear receptors that regulate gene expression in neurons and microglia.
  • “Understanding the mechanism of action of a molecule generally speeds its development and often points the way to broader clinical application,” said Seth Lederman, M.D., Chief Executive Officer of Tonix Pharmaceuticals.
  • “Despite its success in treating depression outside of the U.S. for more than 30 years, tianeptine’s mechanism has remained obscure.
  • “Tianeptine mimics naturally occurring polyunsaturated fatty acid in binding to PPARs.5 When compared to the traditional classes of antidepressants (SSRIs, tricyclics, etc.

BioXcel Therapeutics Announces Positive Top-Line Data from Repeat Dosing of BXCL501 in Phase 1b Multiple Ascending Dose Trial in Healthy Volunteers for Major Depressive Disorder (MDD) Program

Retrieved on: 
Tuesday, May 16, 2023

NEW HAVEN, Conn., May 16, 2023 (GLOBE NEWSWIRE) -- BioXcel Therapeutics, Inc. (Nasdaq: BTAI), a biopharmaceutical company utilizing artificial intelligence approaches to develop transformative medicines in neuroscience and immuno-oncology, today announced positive top-line data from its Phase 1b multiple ascending dose (MAD) trial of BXCL501 (dexmedetomidine) sublingual film. BXCL501 is the Company’s proprietary, orally dissolving film under investigation for the treatment of agitation associated with neuropsychiatric disorders and as a potential adjunctive treatment in Major Depressive Disorder (MDD).

Key Points: 
  • The trial was designed to evaluate the safety and tolerability of repeat dosing of BXCL501 in healthy volunteers as a single agent and in combination with antidepressant duloxetine.
  • “This positive outcome supports the potential market expansion opportunity for our lead asset, BXCL501, into chronic neuropsychiatric disorders,” said Vimal Mehta, CEO of BioXcel Therapeutics.
  • We believe these new data present a transformative opportunity beyond acute treatment for the BXCL501 program, including treatment for MDD.
  • The study’s primary objectives were to assess the safety, tolerability, and pharmacokinetics of BXCL501 in healthy volunteers in multiple ascending doses.

Mindbloom Announces Partnership with SHIFT To Offer Affordable At-Home Ketamine Therapy To Its Employees

Retrieved on: 
Tuesday, April 25, 2023

Mindbloom , the world’s largest provider of ketamine therapy, announced today a partnership with SHIFT , a tech-enabled management consulting firm, to provide at-home ketamine therapy as a benefit to its employees.

Key Points: 
  • Mindbloom , the world’s largest provider of ketamine therapy, announced today a partnership with SHIFT , a tech-enabled management consulting firm, to provide at-home ketamine therapy as a benefit to its employees.
  • Through this partnership, all SHIFT employees will have access to at-home ketamine therapy through Mindbloom for a fraction of the normal price.
  • “I am incredibly proud to partner with employers like SHIFT to increase access to transformative at-home ketamine therapy programs,” said Mindbloom Founder & CEO Dylan Beynon.
  • And in January, Mindbloom announced a partnership with This is Jane Project to offer affordable at-home ketamine therapy to trauma survivors.

Vella Bioscience Inc. Granted First Patent For Use of Cannabinoids in Treating Antidepressant-Induced Female Sexual Dysfunction

Retrieved on: 
Wednesday, March 29, 2023

NEW YORK, March 29, 2023 /PRNewswire/ -- Vella Bioscience Inc. whose Women's Pleasure Serum has been dubbed the "Women's Viagra®," has announced today that the Patent and Trademark Office (USPTO) has granted the brand's first patent. The patent is for the use of cannabinoids in treating Antidepressant-Induced Female Sexual Dysfunction.

Key Points: 
  • whose Women's Pleasure Serum has been dubbed the "Women's Viagra®," has announced today that the Patent and Trademark Office (USPTO) has granted the brand's first patent.
  • The patent is for the use of cannabinoids in treating Antidepressant-Induced Female Sexual Dysfunction.
  • As a company, we bring a certain 'the future-is-now' attitude to women's sexual empowerment and pleasure that is wholly unique."
  • Vella's patent establishes it as a pioneer in the clinical beauty space of female sexual health and wellness and proves its commitment to science and innovation.

Vistagen Announces Positive Data in Fasedienol (PH94B) Phase 3 Open-Label Study in Adults with Social Anxiety Disorder

Retrieved on: 
Wednesday, March 22, 2023

Secondary endpoints in the study included evaluation of the change from baseline on the Liebowitz Social Anxiety Scale (LSAS), which measures SAD patients’ response to anxiety-provoking social and performance situations experienced in their daily lives.

Key Points: 
  • Secondary endpoints in the study included evaluation of the change from baseline on the Liebowitz Social Anxiety Scale (LSAS), which measures SAD patients’ response to anxiety-provoking social and performance situations experienced in their daily lives.
  • The safety and exploratory LSAS results of this Phase 3 open label study build on the safety and LSAS efficacy results from a previous randomized, double-blind, placebo-controlled Phase 2 study of fasedienol in a real-world setting.
  • All prior registration studies for these medications were positive, and all studies used the LSAS as the primary efficacy endpoint.
  • At the time of study closure, study participants had a mean trial exposure of 120 days and a maximum exposure of 320 days.

Black People Less Likely to Receive Dementia-Related Medications

Retrieved on: 
Monday, February 27, 2023

"However, there is limited data for the use of dementia medications that people take at home.

Key Points: 
  • "However, there is limited data for the use of dementia medications that people take at home.
  • Of this group, 3,655 were Black and 12,885 were white.
  • "Black people who saw a neurologist were receiving cholinesterase inhibitors and NMDA antagonists at rates more comparable to white people," said Hawkins.
  • Therefore, Hawkins said it remains unclear how much of the observed disparity is due to physicians prescribing fewer medications to Black people versus other patient-related factors, such as inability to afford medications.