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Claritas Pharmaceuticals Inc V.CLAS.H

Alternate Symbol(s):  CLAZF

Claritas Pharmaceuticals, Inc., formerly Kalytera Therapeutics Inc, is a biotechnology company that is focused on developing R-107 for the treatment of vaccine-resistant coronavirus disease (COVID) strains. The Company’s products in development include R-107 for coronavirus disease and Viral Infections, R-107 and Vaccines, and CLA-1816 for treatment of pain. R-107 is designed to defeat COVID viruses on contact. R-107 targets the Achilles heel of COVID, the spike protein on the surface of the virus. R-107 releases nitric oxide, which attaches to a specific amino acid on the spike protein, thereby disabling the spike protein. The CLA-1816 provides effective pain reduction, without the risks of addiction or respiratory suppression that exist with opioid analgesics. CLA-1816 strongly binds with and activates the alpha3 glycine pain receptor in the spine. The Company has leased a laboratory, office, and archival space in Beverly, Massachusetts.


TSXV:CLAS.H - Post by User

Comment by PTBaileyon Apr 06, 2021 10:17am
154 Views
Post# 32941012

RE:Sedar, Licence Agreement Nov 2020

RE:Sedar, Licence Agreement Nov 2020
whisky11 wrote:

Highlights of the License Agreement

  • R-107 is a liquid prodrug of nitric oxide. Based on the fact that nitric oxide is an approved treatment for acute respiratory failure in newborns, and the clinical evidence of nitric oxide’s antiviral activity against strains of coronavirus, Salzman Group will develop R-107 for treatment of coronavirus and COVID-19 associated lung infection.

  • Following completion of a Phase 1 clinical safety and pharmacokinetic study, Kalytera intends to apply for funding from the U.S. Department of Health and Human Services for the costs of Phase 2 and Phase 3 clinical studies of R-107 in coronavirus and COVID-19 infection.

  • If the application for a new BARDA contract for development of R-107 for treatment of coronavirus and COVID-19 infection is successful, Salzman Group may receive an additional USD $20 million under this BARDA contract.

  • Kalytera expects the Phase 1 clinical safety and pharmacokinetic study to be completed in the first half of 2021.

  • Under the terms of the License Agreement, Kalytera will pay a $1.2 million cash license fee to Salzman Group, and also issue to the former shareholders of Salzman Group 130 million Kalytera common shares. As of September 30, 2020, Kalytera has made partial payments of the $1.2 million cash license fee to the former shareholders of Salzman Group in the total amount of approximately $541,000.

 

Must be disappointing to many when "pumpers" are posting facts. LOL

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