SSRI

Clearmind Medicine Announces International Patent Application for Preventing and Treating Depression

Retrieved on: 
Wednesday, March 27, 2024

Vancouver, Canada, March 27, 2024 (GLOBE NEWSWIRE) -- Clearmind Medicine Inc. (Nasdaq: CMND), (FSE: CWY) (“Clearmind” or the “company”), a biotech company focused on discovery and development of novel psychedelic-derived therapeutics to solve major under-treated health problems, announced that it has submitted its tenth patent application under the international Patent Cooperation Treaty (“PCT”), as part of its ongoing collaboration with SciSparc Ltd. (Nasdaq: SPRC) (“SciSparc”), a specialty clinical-stage pharmaceutical company focusing on the development of therapies to treat disorders of the central nervous system.

Key Points: 
  • The patent applications refer to the novel proprietary composition of Clearmind’s MEAI compound (5-methoxy-2-aminoindane) with Palmitoylethanolamide (“PEA”), the active ingredient of SciSparc’s proprietary CannAmide™, for preventing and/or treating depression.
  • This application was previously filed as provisional patent application with the United States Patent and Trademark Office (“USPTO”).
  • Under our collaboration with SciSparc, we believe that our proprietary drugs can positively impact patients dealing with various forms of depression including treatment resistant depression," stated Dr. Adi Zuloff-Shani, CEO of Clearmind.
  • "We further believe that we have a tremendous opportunity to develop viable alternatives to the current SSRIs for individuals living with depression.

PsyRx Advances Clinical Trial Exploration with Successful Completion of Toxicological Safety Study in Rats

Retrieved on: 
Monday, March 25, 2024

TEL AVIV, Israel, March 25, 2024 /PRNewswire/ -- PsyRx, a leading innovator in pharmaceutical research, is pleased to announce the successful conclusion of the live phase of a toxicological safety study involving the combined treatment of SSRI plus ibogaine.

Key Points: 
  • TEL AVIV, Israel, March 25, 2024 /PRNewswire/ -- PsyRx, a leading innovator in pharmaceutical research, is pleased to announce the successful conclusion of the live phase of a toxicological safety study involving the combined treatment of SSRI plus ibogaine.
  • This groundbreaking study is a pivotal step in the company's ongoing evaluations for conducting a clinical trial in humans, specifically focusing on patients suffering from Major Depressive Disorders (MDD).
  • During the 14 consecutive treatment days, the study examined the safety of administering the combined treatment at three different dose levels—low, medium, and high.
  • The successful completion of this toxicological safety study marks a significant achievement in the pursuit of improving the lives of individuals affected by MDD.

Circular Genomics Strengthens Leadership Team with Key Commercial and Research Hires

Retrieved on: 
Monday, February 26, 2024

ALBUQUERQUE, N.M., Feb. 26, 2024 /PRNewswire/ -- Circular Genomics, the global leader in advancing circular RNA biomarkers for precision psychiatry and neurology, today announced the appointments of Dave Karlander as Chief Commercial Officer and Vishi Srinivasan, Ph.D., as Senior Director of Clinical Research. In these new roles, Karlander will oversee and manage all commercial aspects of the company's operations, including sales, product marketing and managed care; and Dr. Srinivasan will drive the advancement of Circular Genomics' clinical pipeline and strategy for the development of circular RNA-based tests in psychiatric and neurologic disorders.

Key Points: 
  • ALBUQUERQUE, N.M., Feb. 26, 2024 /PRNewswire/ -- Circular Genomics, the global leader in advancing circular RNA biomarkers for precision psychiatry and neurology, today announced the appointments of Dave Karlander as Chief Commercial Officer and Vishi Srinivasan, Ph.D., as Senior Director of Clinical Research.
  • In these new roles, Karlander will oversee and manage all commercial aspects of the company's operations, including sales, product marketing and managed care; and Dr. Srinivasan will drive the advancement of Circular Genomics' clinical pipeline and strategy for the development of circular RNA-based tests in psychiatric and neurologic disorders.
  • "I am delighted to welcome both Dave and Vishi to our leadership team at Circular Genomics," said Dr. Paul Sergeant, Chief Executive Officer of Circular Genomics.
  • "Dave's extensive background in commercial operations, including leading several product launches, will be invaluable during this stage at our company.

Why are so many Australians taking antidepressants?

Retrieved on: 
Thursday, February 8, 2024

Around one in seven Australians take antidepressants; more than 3.5 million of us had them dispensed in 2021–22.

Key Points: 
  • Around one in seven Australians take antidepressants; more than 3.5 million of us had them dispensed in 2021–22.
  • Guidelines mostly recommend antidepressants for more severe depression and anxiety but not as first-line treatment for less severe depression.
  • So why are so many Australians taking antidepressants and why are prescriptions rising?

Enter the antidepressant ‘blockbusters’

  • In the 1990s, pharmaceutical companies heavily promoted new selective serotonin reuptake inhibitors (SSRI) antidepressants, including Prozac (fluoxetine), Zoloft (sertraline) and Lexapro (escitalopram).
  • These drugs were thought to be less dangerous in overdoses and seemed to have fewer side effects than the tricyclic antidepressants they replaced.
  • Pharmaceutical companies marketed SSRIs energetically and often exaggerated their benefits, including by paying “key opinion leaders” – high-status clinicians to promote them.

Why are antidepressants prescribed?

  • GPs also prescribe antidepressants to patients experiencing distress but who don’t have a psychiatric diagnosis.
  • Another, who cried when informed she had breast cancer, was immediately offered a prescription for antidepressants.
  • Most patients believe antidepressants restore a chemical imbalance that underpins depression.
  • Antidepressants are emotional (and sexual) numbing agents – sometimes sedating, sometimes energising.
  • Around half of users have impaired sexual function and for some, this sexual dysfunction persists after stopping antidepressants.

How long do people take antidepressants?

  • Around half of patients who start antidepressants don’t like them and stop within weeks.
  • Of those who do take them for months, many continue to use them indefinitely, often for many years.
  • Read more:
    Antidepressants can cause withdrawal symptoms – here’s what you need to know

We need to adjust how we view mental distress

  • Overprescribing antidepressants is a symptom of our lack of attention to the social determinants of mental health.
  • GPs also need to ensure they discuss with their patients the potential adverse effects of antidepressants, and when and how to safely stop them.
  • But the fundamental problem is social and can only be properly addressed by meaningfully addressing inequality and changing community attitudes to distress.


Jon Jureidini receives research funding from MMRF. He is affiliated with Critical Psychiatry Network Australasia.

Cybin Highlights Recent Topline Results and Outlines Key Upcoming Milestones Across its Clinical Development Programs

Retrieved on: 
Thursday, January 4, 2024

The first quarter of 2024 should be another active and productive period for us, as we advance our clinical programs.

Key Points: 
  • The first quarter of 2024 should be another active and productive period for us, as we advance our clinical programs.
  • For our dDMT programs, we plan to initiate a Phase 2 trial of CYB004 in generalized anxiety disorder (“GAD”),” said Doug Drysdale, Chief Executive Officer of Cybin.
  • “As we look ahead, we see enormous opportunities for progress across our differentiated programs and development pipeline.
  • Upcoming Milestones for dDMT Program:
    Phase 1 topline data for CYB004 expected early Q1 2024.

Human medicines European public assessment report (EPAR): Spravato, esketamine, Date of authorisation: 18/12/2019, Revision: 9, Status: Authorised

Retrieved on: 
Tuesday, January 2, 2024

Human medicines European public assessment report (EPAR): Spravato, esketamine, Date of authorisation: 18/12/2019, Revision: 9, Status: Authorised

Key Points: 


Human medicines European public assessment report (EPAR): Spravato, esketamine, Date of authorisation: 18/12/2019, Revision: 9, Status: Authorised

Mikra Successfully Launches Serenity, an Innovative Mental Health Product for Anxiety

Retrieved on: 
Thursday, November 30, 2023

TORONTO, Nov. 30, 2023 (GLOBE NEWSWIRE) -- Lifeist Wellness Inc. (“Lifeist” or the “Company”) (TSXV: LFST) (FRANKFURT: M5B) (OTCMKTS: LFSWF), a health-tech company that leverages advancements in science and technology to build breakthrough ventures that transform human wellness, is pleased to report that its U.S. biosciences subsidiary Mikra Cellular Sciences Inc. (“Mikra”) has begun sales of Serenity, a natural supplement for addressing symptoms of anxiety.

Key Points: 
  • "We are committed to bringing compelling natural products, backed by the scientific gold standard of randomized controlled trials, to market.
  • Serenity is just such a product, and initial feedback has been overwhelmingly positive."
  • While they are more likely to exhibit psychological concerns compared to previous generations, they are also more likely to be vocal about their mental health concerns and seek help."
  • In a randomized, double-blind clinical trial3 it out-performed paroxetine (PaxilTM), a frontline SSRI prescribed for the management of generalized anxiety disorder.

Mikra Introduces Serenity, an Innovative Mental Health Product for Anxiety, Available for Purchase on Black Friday

Retrieved on: 
Thursday, November 16, 2023

"We are delighted to bring Serenity to market ahead of schedule and in time for Black Friday, the busiest shopping day of the year," said Meni Morim, CEO of Lifeist. "Serenity ships with a full 30-day supply in every bottle, as compared to the typical 7- or 14-day supply sold in competing lavender-based products. We are confident that our value proposition, combined with a consistent GCMS-verified dose1 of the active ingredient and the gentle flavor profile provided by our proprietary polyterpene blend, will offer customers an attractive natural alternative -- powered by science2 -- to counter anxiety."

Key Points: 
  • "We are delighted to bring Serenity to market ahead of schedule and in time for Black Friday, the busiest shopping day of the year," said Meni Morim, CEO of Lifeist.
  • "Serenity ships with a full 30-day supply in every bottle, as compared to the typical 7- or 14-day supply sold in competing lavender-based products.
  • In a randomized, double-blind clinical trial it out-performed paroxetine (PaxilTM), a frontline SSRI prescribed for the management of generalized anxiety disorder.
  • Lifeist looks forward to bringing this innovative solution to market, and to continuing to build a robust, science-based pipeline of products in 2024.

Lifeist's Mikra Completes Formulation of Innovative Mental Health Product for Anxiety 

Retrieved on: 
Thursday, November 2, 2023

This innovation complements our successful CELLF product, reflecting our commitment to advancing holistic wellness solutions."

Key Points: 
  • This innovation complements our successful CELLF product, reflecting our commitment to advancing holistic wellness solutions."
  • "Anxiety disorders are widespread, affecting 40 million adults in the U.S. alone, yet a significant portion of this population remains untreated.
  • Serenity is poised to make a meaningful impact in enhancing mental well-being, aligning with our vision of improving lives through cellular health."
  • Mikra takes pride in introducing Serenity, which will be available for sale on weareMikra.com before the December holiday season.

Pioneering Phase III Clinical Trial Investigates Multiple Potential Long-COVID Treatments

Retrieved on: 
Thursday, November 2, 2023

The trial was designed by researchers at McMaster University in Hamilton, Canada, and is aimed at addressing the persisting challenges posed by Long-COVID.

Key Points: 
  • The trial was designed by researchers at McMaster University in Hamilton, Canada, and is aimed at addressing the persisting challenges posed by Long-COVID.
  • As a multi-center study beginning with 1,500 patients, the trial will rigorously assess the efficacy of multiple potential treatment options – beginning with fluvoxamine and metformin – in alleviating the symptoms associated with Long-COVID.
  • The trial will leverage state-of-the-art data management via an EDC developed by Yonalink, to ensure the highest caliber of data integrity.
  • The new approach seeks to swiftly identify effective Long-COVID-19 treatments and assess comparative efficacy without compromising the rigorous standards of a randomized clinical trial.