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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

Post by maverick2004on Mar 04, 2021 7:01am
359 Views
Post# 32712719

big news

big news

 

Kalytera Therapeutics, Beetlebund licence agreement

 

2021-03-03 20:37 ET - Property Agreement

 

The TSX Venture Exchange has accepted for filing documentation a licence agreement dated March 30, 2018, between the company and Beetlebung Pharma Ltd. Pursuant to the terms of the agreement, the company has obtained a worldwide exclusive licence with respects to its cannabinoid-based compound with the vendor, and with which the vendor has built a development program for the treatment of acute and chronic pain. As total consideration, the company has decided to provide the vendor with a variety of milestone payments described as follows:

 

  • An aggregate set of cash payments equivalent to approximately $4,325,000 (U.S.) is set to be paid upon completing specific milestones as per the terms of the agreement subject to additional sublicensing fees;
  • A success fee will be payable upon receiving approval by the U.S. Food and Drug Administration (FDA) with consideration to the vendor satisfied through the issuance of an aggregate of 6.5 million common shares and a cash payment equal to:
    • The amount by which the closing price of the company's shares on the exchange on the date on which FDA approval is announced multiplied by 5 per cent of the company's issued and outstanding shares at that time exceeds the value of the success fee shares.

 

Under the terms of the agreement, the vendor will also be eligible to reserve a 5-per-cent royalty payment from the net sales of the cannabinoid-based compound in each country in which the applicable patent is covered by. In addition, the company will be liable to pay a cash payment of $150,000 (U.S.) upon the issuance of the first patent in each the following jurisdictions:

 

  1. The United States;
  2. Japan;
  3. Any one of the five major European countries mentioned below:
    • Germany;
    • France;
    • The United Kingdom;
    • Spain;
    • Italy.

 

 

Insider/pro group participation:  none

 

For more information, please reference the company's news releases dated April 13, 2018, and Feb. 24, 2021.

© 2021 Canjex Publishing Ltd. All rights reserved.

 
 
 
 
 
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