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Sona Nanotech Inc C.SONA

Alternate Symbol(s):  SNANF

Sona Nanotech Inc. is a nanotechnology life sciences company, which is engaged in developing targeted hyperthermia therapy. The Company has developed multiple methods for the manufacturing of various types of gold nanoparticles (GNR). It is engaged in research and development of its technology for use in multiplex diagnostic testing platforms and advanced biomedical applications. Its gold nanotechnologies are adapted for use in applications, as a safe and delivery system for multiple medical treatments, for the approval of various regulatory boards, including Health Canada and the Food and Drug administration (FDA). Its gold nanorod particles are manufactured without the use of cetyltrimethylammonium bromide (CTAB), eliminating the toxicity risks associated with the use of other gold nanorod technologies in medical applications. The Company is focused on the development of a pre-clinical nanomedical therapy for the treatment of cancer using its biocompatible GNR.


CSE:SONA - Post by User

Comment by Pandoraon Dec 07, 2020 5:56pm
214 Views
Post# 32054530

RE:GREATER than 99% accuracy - Covid-19 Antibody test....(SQD)

RE:GREATER than 99% accuracy - Covid-19 Antibody test....(SQD)
Therma Bright has released news on it's saliva test and are proclaiming the 80% sensitivity level.

"The minimum standard for home-use approval of rapid antigen tests is 80% sensitivity with both FDA under Emergency Use Authorization ("EUA") and Health Canada under the Interim Order. Therma and its partners are pleased to achieve the minimum threshold for approval with regulatory agencies."

Sona's test was above 80% was it not? And I thought that was not good enough for either Health Canada or the FDA?


Toronto, Ontario--(Newsfile Corp. - December 7, 2020) - Therma Bright Inc. (TSXV: THRM) ("Therma" or the "Company"), a progressive medical device technology company, is pleased to announce the preliminary results achieved during the feasibility studies indicate a test sensitivity of 80% and a specificity of over 90% for Therma's CoviSafe™ rapid test for detecting SARS-CoV-2 in saliva.

Therma entered into an agreement with nanoComposix, a developer and manufacturer of rapid diagnostic tests to perform feasibility studies with a short list of polypeptides identified by Therma's strategic partners. Preliminary studies have identified a number of polypeptide pairs that will be tested in the coming weeks in human saliva samples containing the SARS CoV-2 virus.

It is expected that the performance will be improved once the final pair of polypeptide reagents is optimized. The minimum standard for home-use approval of rapid antigen tests is 80% sensitivity with both FDA under Emergency Use Authorization ("EUA") and Health Canada under the Interim Order. Therma and its partners are pleased to achieve the minimum threshold for approval with regulatory agencies.

In addition to the selection and optimization of the best polypeptide pair of reagents, nanoComposix will assist Therma and its partners in developing a proprietary test cartridge and saliva collection device that will be cost effective, easy to use, secure and suited for routine home-use testing.

Therma will procure up to 300 prototype tests from one of its suppliers to undertake initial testing with selected sites in Ontario. The initial testing of the CoviSafe™ test will be for symptomatic patients. Therma is working with Public Health Ontario to identify sites in the Province to conduct preliminary testing and evaluation of CoviSafe™. Testing is expected to start before year end, but because of potential delays due to the holidays, may extend into January.

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