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Theralase Technologies Inc. V.TLT

Alternate Symbol(s):  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

Bullboard Posts
Comment by Hempdocon Jun 23, 2020 9:12pm
88 Views
Post# 31183842

RE:The Erosion Of Science/Research...

RE:The Erosion Of Science/Research...
Hempdoc wrote:

for the betterment of society, or for the enrichment of Big Pharma & all of those who have their hands in Pharm's deep pockets (academicians, so-called independent experts, the MSM)? So many instances where HCQ is being intentionally maligned in the research/clinical trial world...sad reality.  Also, just because a study may be randomized/placebo-controlled/double-blinded doesn't make it valid, or even on point.  You can tailor any study to your (Big Pharma's) desired outcome...like practically overdosing HCQ cohorts in already hospitalized/critically ill/high-risk patients (many with cardiac disease/failure).  It's not too difficult to tarnish a drug if there's enough $ incentive.

One simply needs to keep his eye on legitimate studies that not only "properly dose", but also "properly test/utilize" HCQ as a "combination" drug (not monotherapy) in an "ambulatory" setting. "Early use" is key for any anti-viral in general...once you wait until someone is critically ill, oxygen-requiring, mechanically ventilated or in the ARD stage, the viral load is much too high & "any" anti-viral will show little to no benefit in terms of reducing mortality.  Unfortunately, too few studies exist looking at HCQ properly.  

https://healthimpactnews.com/2020/editors-of-the-lancet-and-the-new-england-journal-of-medicine-pharmaceutical-companies-are-so-financially-powerful-they-pressure-us-to-accept-papers/



Forgot to mention the FDA/CDC-Big Pharma connection.  TLT's battle won't necessarily be the science nor the financing imo.   With IND approval in hand, I would expect to see a significant increase in US accruals/treated patients later this year.  If not, my guess is many patients will be steered towards Keytruda & the like.  Accrual is our key to the promised land.  Building relationships with community-based organizations/physicians would be a good start.  Let's hope our TMO is getting the job done...imo a total of 4 to 6 committed trial sites in the US may be a money-wise move & more than enough additional data for early approval if the science continues to prove itself.

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