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Theralase Technologies Inc. V.TLT

Alternate Symbol(s):  V.TLT.WT | TLTFF

Theralase Technologies Inc. is a Canada-based clinical-stage pharmaceutical company. The Company is engaged in the research and development of light activated compounds and their associated drug formulations. The Company operates through two divisions: Anti-Cancer Therapy (ACT) and Cool Laser Therapy (CLT). The Anti-Cancer Therapy division develops patented, and patent pending drugs, called Photo Dynamic Compounds (PDCs) and activates them with patent pending laser technology to destroy specifically targeted cancers, bacteria and viruses. The CLT division is responsible for the Company’s medical laser business. The Cool Laser Therapy division designs, develops, manufactures and markets super-pulsed laser technology indicated for the healing of chronic knee pain. The technology has been used off-label for healing numerous nerve, muscle and joint conditions. The Company develops products both internally and using the assistance of specialist external resources.


TSXV:TLT - Post by User

Comment by ScienceFirston Dec 07, 2020 5:14pm
59 Views
Post# 32054370

RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:Hahaha... Rudy's got it

RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:Hahaha... Rudy's got itBunge, Bunge, Bunge ...

Journal Publisher Concerned over Hydroxychloroquine Study

The report by Didier Raoult and colleagues that examined the use of the anti-malarial drug in a small number of COVID-19 patients receives criticism from the very society that published it.

Elsevier, copublisher of the International Journal of Antimicrobial Agents, issued a statement on April 11 that “additional independent peer review is ongoing to ascertain whether concerns about the research content of the paper have merit.”

With little evidence to back him, President Donald Trump has championed an anti-malarial drug called hydroxychloroquine as a treatment for COVID-19. His endorsement has led to hoarding and shortages for lupus patients who rely on the medicine. 

While it may turn out to be an effective drug—and a number of clinical trials are aiming to find out—the clinical data so far are preliminary and, it turns out, possibly problematic.

According to a statement issued April 3 by the International Society of Antimicrobial Chemotherapy (ISAC), the vanguard study cited by Trump and others in their endorsement of hydroxychloroquine “does not meet the Society’s expected standard, especially relating to the lack of better explanations of the inclusion criteria and the triage of patients to ensure patient safety.” 

The ISAC publishes the International Journal of Antimicrobial Agents, where Didier Raoult of Aix-Marseille Universit and colleagues reported their findings on a trial of three dozen patients, 20 of whom took hydroxychloroquine (six of these patients also received an antibiotic). The statement from ISAC notes that the journal’s editor in chief is in agreement with the society’s concern, although the society defends the peer review process that the paper went through. “Although ISAC recognises it is important to help the scientific community by publishing new data fast, this cannot be at the cost of reducing scientific scrutiny and best practices,” the statement adds.
 

Elisabeth Bik, a microbiologist who works to improve the quality of the scientific literature, noted in a blog post a number of issues with the study after it first appeared as a preprint, including confounders, a lack of randomization, and reported data that did not match the plan outlined in a clinical trial registry.

Another preprint by Raoult’s group of 80 COVID-19 patients who received hydroxychloroquine and the antibiotic azithromycin similarly received criticism for a lack of control group, the inclusion of asymptomatic carriers, and questionable results. For instance, Derek Lowe points out in his blog that 10 patients went from a positive to negative nasal swab test between the first and second day of treatment. “That seems hard to believe, unless they were already close to the cutoff, but here’s a big problem with the preprint: we do not have individual patient data,” he writes.





So you have no proof that it works apart from phony studies that don't as Trump would have forced the approval.  You know how he is, when he wants something.

Moreover, Trump, Gugliania, etc ... took all the different formulas including your and they caught it. 

We cannot trust your libertarian views, especlially with the number of cases and you that minimized the threat of this virus for months.  You even mentioned argued that it was 10x less deadly than regular flu, not even knowing how to read officials numbers!
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