Molecular neuroscience

Insomnia Data 2020: US Leads in Global Insomnia Clinical Trials, Germany Leads Major European Markets and Japan Has Top Spot in Asia

Retrieved on: 
Thursday, May 21, 2020

It is estimated that Asia had the largest number of prevalent cases in 2017 (675.7 million cases).

Key Points: 
  • It is estimated that Asia had the largest number of prevalent cases in 2017 (675.7 million cases).
  • The approved drugs in the insomnia space target GABA-A receptor, hypocretin/orexin receptor, chloride channel 2, chloride, melatonin receptor, histamine H1 receptor, and potassium channels.
  • Germany leads the major European markets, while Japan has the top spot in Asia.
  • Takeda leads the industry sponsors with the highest overall number of clinical trials for insomnia, followed by Merck & Co.

Protecting a Most Precious Asset: GABA Proved to Fortify Cognitive Health in Human Trials

Retrieved on: 
Tuesday, March 31, 2020

They want to have agency over the state of their mental health as they age, as they do their physical health.

Key Points: 
  • They want to have agency over the state of their mental health as they age, as they do their physical health.
  • The benefits of the naturally-occurring amino acid neurotransmitter GABA [-Aminobutyric acid], found across a range of healthful foods, have never really been in doubt.
  • It has long been known that a decreased systemic level of GABA is associated with the presence of Parkinsons disease, epilepsy, Huntingtons chorea, Alzheimers disease, and schizophrenia.
  • The current studies published by Pharma Foods International offer the promise that a naturally-occurring, naturally derived supplement, GABA, may lead the way.

2020 Market Spotlight: Insomnia -- Eisai Buys Out Global Rights to Lemborexant - ResearchAndMarkets.com

Retrieved on: 
Monday, March 30, 2020

It is estimated that Asia had the largest number of prevalent cases in 2017 (675.7 million cases).

Key Points: 
  • It is estimated that Asia had the largest number of prevalent cases in 2017 (675.7 million cases).
  • The approved drugs in the insomnia space target GABA-A receptor, hypocretin/orexin receptor, chloride channel 2, chloride, melatonin receptor, histamine H1 receptor, and potassium channels.
  • The largest proportion of industry-sponsored drugs in active clinical development for insomnia are in Phase III, with only one drug in the NDA/BLA phase.
  • Takeda leads the industry sponsors with the highest overall number of clinical trials for insomnia, followed by Merck & Co.

Isotopia Molecular Imaging and Eckert & Ziegler to Start Partnership for Prostate Cancer Imaging

Retrieved on: 
Thursday, February 13, 2020

PETACH TIKVA, Israel, Feb. 13, 2020 /PRNewswire/ -- Isotopia Molecular Imaging is pleased to announce that is has entered into a development partnership with Eckert & Ziegler for the development of its PSMA-11-Kit for prostate cancer imaging.

Key Points: 
  • PETACH TIKVA, Israel, Feb. 13, 2020 /PRNewswire/ -- Isotopia Molecular Imaging is pleased to announce that is has entered into a development partnership with Eckert & Ziegler for the development of its PSMA-11-Kit for prostate cancer imaging.
  • Under the terms of the agreement, E&Z and Isotopia will partner to finalize the development of Isotopia's68Ga-HBED-CC-PSMA (68Ga-PSMA-11) kit (Kit), a technology for imaging and staging of prostate cancer.
  • Isotopia's head of Business development, Keren Moshkoviz stated, "We are excited in taking another significant step towards making prostate cancer imaging more accessible.
  • PSMA-11 radiolabeled with68Ga (gallium) is a convenient and clinically efficient approach to imaging prostate cancer with Positron Emission Tomography (PET).

Prothena Reports Fourth Quarter and Full Year 2019 Financial Results, and Provides Financial Guidance and R&D Update

Retrieved on: 
Wednesday, February 12, 2020

In addition, the Company provided 2020 financial guidance and an update on its R&D programs.

Key Points: 
  • In addition, the Company provided 2020 financial guidance and an update on its R&D programs.
  • In 2019, we continued to advance our pipeline of novel investigational therapeutics towards key milestones, said Gene Kinney, Ph.D., President and Chief Executive Officer of Prothena.
  • Initiated cell line development of a lead candidate in the proprietary preclinical A (Amyloid beta) program in the fourth quarter of 2019.
  • As of December31, 2019, Prothena had $378.4 million in cash, cash equivalents and restricted cash and no debt.

Sosei Heptares: Significant Progress by Orexia and Inexia With Orexin Agonist Program Triggers Next Tranche of Funding From Medicxi

Retrieved on: 
Tuesday, January 14, 2020

Mario Alberto Accardi Ph.D., CEO of Orexia and Inexia, commented:"We have assembled a unique orexin modulator drug discovery and design engine at Orexia and Inexia, based around Sosei Heptares' SBDD and GPCR technology.

Key Points: 
  • Mario Alberto Accardi Ph.D., CEO of Orexia and Inexia, commented:"We have assembled a unique orexin modulator drug discovery and design engine at Orexia and Inexia, based around Sosei Heptares' SBDD and GPCR technology.
  • This significant and exciting progress has triggered the investment of further committed funds from Medicxi that will be deployed to rapidly advance these highly promising molecules towards the clinic."
  • Dr. Malcolm Weir, Executive Vice President, Research & Early Development at Sosei Heptares, added: "We are very pleased with the progress being made in the orexin agonist program in collaboration with Orexia and Inexia and with support and funding from Medicxi.
  • Orexia and Inexia are focused on developing Orexin OX1 and OX2 positive modulators and products derived therefrom, including dual OX1/OX2 agonists, targeting neurological diseases including narcolepsy.

Sosei Heptares: Significant Progress by Orexia and Inexia With Orexin Agonist Program Triggers Next Tranche of Funding From Medicxi

Retrieved on: 
Tuesday, January 14, 2020

Mario Alberto Accardi Ph.D., CEO of Orexia and Inexia, commented:"We have assembled a unique orexin modulator drug discovery and design engine at Orexia and Inexia, based around Sosei Heptares' SBDD and GPCR technology.

Key Points: 
  • Mario Alberto Accardi Ph.D., CEO of Orexia and Inexia, commented:"We have assembled a unique orexin modulator drug discovery and design engine at Orexia and Inexia, based around Sosei Heptares' SBDD and GPCR technology.
  • This significant and exciting progress has triggered the investment of further committed funds from Medicxi that will be deployed to rapidly advance these highly promising molecules towards the clinic."
  • Dr. Malcolm Weir, Executive Vice President, Research & Early Development at Sosei Heptares, added: "We are very pleased with the progress being made in the orexin agonist program in collaboration with Orexia and Inexia and with support and funding from Medicxi.
  • Orexia and Inexia are focused on developing Orexin OX1 and OX2 positive modulators and products derived therefrom, including dual OX1/OX2 agonists, targeting neurological diseases including narcolepsy.

Alzheon Publication Defines New Path for 2nd Generation Anti-Amyloid Drugs for Alzheimer’s Disease, Supporting Launch of Phase 3 Study with ALZ-801 Oral Tablet

Retrieved on: 
Wednesday, November 6, 2019

This improved pharmacological profile will enable anti-amyloid drugs to achieve robust and meaningful clinical efficacy, and to realize the full potential of this most promising class of Alzheimers medicines.

Key Points: 
  • This improved pharmacological profile will enable anti-amyloid drugs to achieve robust and meaningful clinical efficacy, and to realize the full potential of this most promising class of Alzheimers medicines.
  • These insights have also guided Alzheon strategy in developing ALZ-801, which is the only remaining Phase 3 candidate with the attributes required for the next generation of anti-amyloid therapies.
  • Furthermore, the lack of selectivity leads to clearance of amyloid plaques that may contribute to vascular injury resulting in brain edema and microhemorrhages.
  • Our lead Alzheimers clinical candidate, ALZ-801 , is a Phase 3-ready, first-in-class, small molecule oral inhibitor of beta amyloid aggregation and neurotoxicity hallmarks of Alzheimers disease.

VistaGen Therapeutics Announces Last Patient Completes Dosing in the ELEVATE Phase 2 Clinical Study of AV-101 for Major Depressive Disorder

Retrieved on: 
Tuesday, October 8, 2019

The Company remains on track to report top line results of the ELEVATE study before the end of 2019.

Key Points: 
  • The Company remains on track to report top line results of the ELEVATE study before the end of 2019.
  • The NMDA receptor is a pivotal receptor in the brain and abnormal NMDA function is associated with numerous CNS diseases and disorders.
  • AV-101 is an oral prodrug of 7-Cl-KYNA, a potent and selective full antagonist of the glycine coagonist site of the NMDA receptor.
  • The primary endpoint of the ELEVATE study is the change from baseline on the Montgomery-sberg Depression Rating Scale (MADRS-10) total score.

Further Data Review Shows Major Clinical Benefits From Veyonda®

Retrieved on: 
Monday, September 30, 2019

The three endpoints used to measure anti-cancer effect all showed a benefit from combining Veyonda with 177Lu-PSMA therapy.

Key Points: 
  • The three endpoints used to measure anti-cancer effect all showed a benefit from combining Veyonda with 177Lu-PSMA therapy.
  • Adding Veyonda to 177Lu-PSMA therapy almost doubled the PSA response (69% with Veyonda vs 36% with 177Lu-PSMA alone).
  • In summary, combination therapy of Veyonda and 177Lu-PSMA therapy shows benefits to patients well above that with 177Lu-PSMA therapy alone and underscores the Companys confidence in Veyonda eventually becoming a standard drug in the management of prostate cancer.
  • Following safety data review of the first cohort (400 mg Veyonda), the dose for patients 9-16 was escalated to 800mg Veyonda for 10 days.