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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 Random1234on Feb 25, 2021 8:11pm
240 Views
Post# 32667662

Next steps in the development of R-107

Next steps in the development of R-107

from Claritas Wesite
"The immediate next step is to complete a Phase 1 clinical study to demonstrate that R-107 is safe in humans. This will be followed by Phase 2 and Phase 3 clinicals studies. It is anticipated that the FDA will allow an expedited clinical development pathway for R-107 in this indication.

  • R-107 is Phase 1 Ready Right Now: To date, the development of R-107 has been largely funded by approximately $15 million of federal funds that were provided to Salzman Group under a grant provided by the U.S. Department of Health and Human Services.  In addition to this $15 million of federal funding, Salzman Group also invested approximately $5 million of its own funds in the preclinical development of R-107. At this point all pre-IND work is complete, including safety studies in two large animal species.
  • Phase 1 Clinical Study: Claritas plans to submit an Investigational New Drug Application (IND) to the Australian Therapeutic Goods Administration (TGA) and the U.S Food and Drug Administration (FDA) in support of the first-in-human Phase 1 clinical study. This Phase 1 study of intramuscular R-107 will be conducted at CMAX, a clinical contract research organization located at Royal Adelaide Hospital in Australia."
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