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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 AngelaLon Jan 01, 2022 11:14pm
228 Views
Post# 34276809

RE:RE:RE:RE:RE:Upside move

RE:RE:RE:RE:RE:Upside move Claritas raised funds recently from Obsidian. So presumably they have the resources to advance and carry out the Australian Phase 1 trial that they have described. If this is indeed the case then that trial will transform the company into a clinical-stage enterprise. The current sp is depressed because it includes the insecurity that the company may not have the resources or ability to start clinical trials. Once the company does in fact start the trial then this uncertainty would be removed and the sp should rebound strongly, initially to a dollar I think. If the trial concludes successfully, showing safety (a relatively low bar) then the market cap almost reflexy should hit US$40-100M. Given the number of outstanding shares, this should equal a sp on the TSXV of $1.25-3.12. It could go higher if the company has a better balance sheet and/or if the perception is that the clinical indication is an important unmet medical need and the technology is broadly applicable, ie a platform technology of a paradigm shift in treatment approach. I believe that all of those criteria could be met. If so, I think it's a relatively conservative expectation to anticipate a 6-15 fold ROI in the next 6 months. Delays or a safety failure will temper that expectation. 
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